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1 | Source, April 18: | https://clinicaltrials.gov/ct2/results?cond=COVID-19 | ||||||||||||||||||||||||
2 | URL | Phases | Primary Completion Date | Length (days) | Status | Interventions | Study Type | Enrollment | Title | Acronym | Study Results | Conditions | Outcome Measures | Sponsor/Collaborators | Age | Funded Bys | Study Designs | Completion Date | First Posted | Start Date | Last Update Posted | Locations | Study Documents | NCT Number | ||
3 | https://ClinicalTrials.gov/show/NCT04280705 | Phase 3 | 4/1/2023 | 1,135 | https://docs.google.com/spreadsheets/d/15r-EqvDTJJLMhOaEzPjrEcFAMPPPk9-FTgdt-qWG6lY/edit#gid=2022203840&range=2:2 | Drug: Remdesivir | Interventional | 440 | Adaptive COVID-19 Treatment Trial (ACTT) | No Results Available | Corona Virus Infection | Percentage of subjects reporting each severity rating on an 8-point ordinal scale|Change from baseline in alanine transaminase (ALT)|Change from baseline in aspartate transaminase (AST)|Change from baseline in creatinine|Change from baseline in glucose|Change from baseline in hemoglobin|Change from baseline in platelets|Change from baseline in prothrombin time (PT)|Change from baseline in total bilirubin|Change from baseline in white blood cell count with differential|Change in National Early Warning Score (NEWS) from baseline|Clinical status using ordinal scale|Cumulative incidence of Grade 3 and 4 adverse events (AEs)|Cumulative incidence of serious adverse events (SAEs)|Discontinuation or temporary suspension of infusions|Duration of hospitalization|Duration of new non-invasive ventilation or high flow oxygen use|Duration of new oxygen use|Duration of new ventilator or extracorporeal membrane oxygenation (ECMO) use|Incidence of new non-invasive ventilation or high flow oxygen use|Incidence of new oxygen use|Incidence of new ventilator or extracorporeal membrane oxygenation (ECMO) use|Mean change in the ordinal scale|Number of non-invasive ventilation/high flow oxygen free days|Number of oxygenation free days|Subject 14-day mortality|Subject 28-day mortality|Time to an improvement of one category using an ordinal scale|Time to an improvement of two categories using an ordinal scale|Time to discharge or to a National Early Warning Score (NEWS) of </= 2 and maintained for 24 hours, whichever occurs first|Ventilator/extracorporeal membrane oxygenation (ECMO) free days | National Institute of Allergy and Infectious Diseases (NIAID) | 18 Years to 99 Years (Adult, Older Adult) | NIH | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Investigator)|Primary Purpose: Treatment | 4/1/2023 | 2/21/2020 | 2/21/2020 | 3/27/2020 | University of Alabama at Birmingham School of Medicine - Infectious Disease, Birmingham, Alabama, United States|University of California San Diego Health - Jacobs Medical Center, La Jolla, California, United States|University of California Los Angeles Medical Center - Westwood Clinic, Los Angeles, California, United States|University of California Irvine Medical Center - Infectious Disease, Orange, California, United States|VA Palo Alto Health Care System - Infectious Diseases, Palo Alto, California, United States|Stanford University - Stanford Hospital and Clinics - Pediatrics - Infectious Diseases, Palo Alto, California, United States|University of California Davis Medical Center - Internal Medicine - Infectious Disease, Sacramento, California, United States|Naval Medical Center San Diego - Infectious Disease Clinic, San Diego, California, United States|University of California San Francisco - Zuckerberg San Francisco General Hospital - Division of Human Immunodeficiency Virus, Infectious Disease, and Global Medicine, San Francisco, California, United States|Denver Health Division of Hospital Medicine - Main Campus, Denver, Colorado, United States|Emory Vaccine Center - The Hope Clinic, Decatur, Georgia, United States|Northwestern Hospital - Infectious Disease, Chicago, Illinois, United States|University of Illinois at Chicago College of Medicine - Division of Infectious Diseases, Chicago, Illinois, United States|University of Maryland School of Medicine - Center for Vaccine Development - Baltimore, Annapolis, Maryland, United States|Johns Hopkins Hospital - Medicine - Infectious Diseases, Baltimore, Maryland, United States|National Institutes of Health - Clinical Center, National Institute of Allergy and Infectious Diseases Laboratory Of Immunoregulation, Clinical Research Section, Bethesda, Maryland, United States|Walter Reed Army Institute of Research - Clinical Trials Center, Silver Spring, Maryland, United States|Massachusetts General Hospital - Infectious Diseases, Boston, Massachusetts, United States|University of Minnesota Medical Center, Fairview - Infectious Diseases and International Medicine, Minneapolis, Minnesota, United States|Saint Louis University - Center for Vaccine Development, Saint Louis, Missouri, United States|University of Nebraska Medical Center - Infectious Diseases, Omaha, Nebraska, United States|Montefiore Medical Center - Infectious Diseases, Bronx, New York, United States|New York University School of Medicine - Langone Medical Center - Microbiology - Parasitology, New York, New York, United States|University of Rochester Medical Center - Vaccine Research Unit, Rochester, New York, United States|Duke Human Vaccine Institute - Duke Vaccine and Trials Unit, Durham, North Carolina, United States|Hospital of the University of Pennsylvania - Infectious Diseases, Philadelphia, Pennsylvania, United States|Vanderbilt University Medical Center - Infectious Diseases, Nashville, Tennessee, United States|Brooke Army Medical Center, Fort Sam Houston, Texas, United States|University of Texas Medical Branch - Division of Infectious Disease, Galveston, Texas, United States|Baylor College of Medicine - Molecular Virology and Microbiology, Houston, Texas, United States|University of Texas Health Science Center at San Antonio - Infectious Diseases, San Antonio, Texas, United States|Naval Medical Center Portsmouth - Infectious Disease Division, Portsmouth, Virginia, United States|EvergreenHealth Infectious Disease Service, Kirkland, Washington, United States|The University of Washington - Virology Research Clinic, Seattle, Washington, United States|Providence Sacred Heart Medical Center, Spokane, Washington, United States|Madigan Army Medical Center - Infectious Disease Clinic, Tacoma, Washington, United States|National Center for Global Health and Medicine Hospital - Disease Control and Prevention Center, Tokyo, Japan|Seoul National University Bundang Hospital - Division of Infectious Diseases, Bundang-gu Seongnam-si, Gyeonggi-do, Korea, Republic of|Seoul National University Hospital, Seoul, Jongno-gu, Korea, Republic of|National Centre for Infectious Diseases (NCID), Singapore, Singapore | NCT04280705 | ||||
4 | https://ClinicalTrials.gov/show/NCT04322786 | 5/31/2016 | 6,725 | Active, not recruiting | Drug: ACE inhibitor | Observational | 1302508 | The Use of Angiotensin Converting Enzyme Inhibitors and Incident Respiratory Infections, Are They Harmful or Protective? | No Results Available | Covid-19, Coronavirus, Angiotensin Converting Enzyme Inhibitors, Influenza, Electronic Health Records, Epidemiology, Comorbidity, Incidence, United Kingdom | Incidence of influenza | University College, London | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Prospective | 3/31/2020 | 3/26/2020 | 1/1/1998 | 3/26/2020 | NCT04322786 | ||||||
5 | https://ClinicalTrials.gov/show/NCT04302688 | 2/10/2020 | 62 | Completed | Observational | 669 | Accurate Classification System for Patients With COVID-19 Pneumonitis | No Results Available | Pneumonitis | survival status | Renmin Hospital of Wuhan University | Child, Adult, Older Adult | Other | Observational Model: Other|Time Perspective: Retrospective | 3/4/2020 | 3/10/2020 | 12/10/2019 | 3/10/2020 | Renmin Hospital of Wuhan University, Wuhan, Hubei, China | NCT04302688 | ||||||
6 | https://ClinicalTrials.gov/show/NCT04284046 | 2/18/2020 | 18 | Completed | Other: CT score | Observational | 39 | CT Scores Predict Mortality in 2019-nCoV Pneumonia | No Results Available | CT Scores Predict Mortality in 2019-nCoV Pneumonia | 7-day mortality | Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine | Child, Adult, Older Adult | Other | Observational Model: Cohort|Time Perspective: Retrospective | 2/18/2020 | 2/25/2020 | 1/31/2020 | 2/25/2020 | Wuhan third hospital, Wuhan, Hubei, China | NCT04284046 | |||||
7 | https://ClinicalTrials.gov/show/NCT04285801 | 2/25/2020 | 11 | Completed | Observational | 8 | Critically Ill Patients With COVID-19 in Hong Kong: a Multicentre Observational Cohort Study | No Results Available | COVID-19 | 28 day mortality|vasopressor days|days on mechanical ventilation|sequential organ function assessment score|ECMO use|percentage nitric oxide use|percentage free from oxygen supplement | Chinese University of Hong Kong | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Case-Only|Time Perspective: Retrospective | 2/25/2020 | 2/26/2020 | 2/14/2020 | 3/10/2020 | Pamela Youde Nethersole Eastern Hospital, Hong Kong, Hong Kong|Prince of Wales Hospital, Hong Kong, Hong Kong|Princess Margaret Hospital, Hong Kong, Hong Kong | NCT04285801 | ||||||
8 | https://ClinicalTrials.gov/show/NCT04293692 | Not Applicable | 2/25/2020 | 1 | Withdrawn | Biological: UC-MSCs|Other: Placebo | Interventional | 0 | Therapy for Pneumonia Patients iInfected by 2019 Novel Coronavirus | No Results Available | COVID-19 | Size of lesion area by chest imaging|Blood oxygen saturation|Rate of mortality within 28-days|Sequential organ failure assessment|Side effects in the UC-MSCs treatment group|Electrocardiogram, the changes of ST-T interval mostly|Concentration of C-reactive protein C-reactive protein, immunoglobulin|CD4+ and CD8+ T cells count|Concentration of the blood cytokine (IL-1β, IL-6, IL-8,IL-10,TNF-α)|Concentration of the myocardial enzymes | Puren Hospital Affiliated to Wuhan University of Science and Technology|Wuhan Hamilton Bio-technology Co., Ltd | 18 Years to 75 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Triple (Participant, Care Provider, Outcomes Assessor)|Primary Purpose: Treatment | 2/25/2020 | 3/3/2020 | 2/24/2020 | 3/18/2020 | Puren Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, Hubei, China | NCT04293692 | ||||
9 | https://ClinicalTrials.gov/show/NCT04261517 | Phase 3 | 2/25/2020 | 19 | Completed | Drug: Hydroxychloroquine | Interventional | 30 | Efficacy and Safety of Hydroxychloroquine for Treatment of Pneumonia Caused by 2019-nCoV ( HC-nCoV ) | No Results Available | Pneumonia, Pneumocystis|Coronavirus | The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 3|The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 5|The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 7|The mortality rate of subjects at weeks 2|Number of participants with treatment-related adverse events as assessed by CTCAE v5.0|The critical illness rate of subjects at weeks 2 | Shanghai Public Health Clinical Center | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 2/25/2020 | 2/7/2020 | 2/6/2020 | 3/24/2020 | Shanghai Public Health Clinical Center, Shanghai, Shanghai, China|Shanghai Public Health Clinical Center, Shanghai, Shanghai, China | NCT04261517 | ||||
10 | https://ClinicalTrials.gov/show/NCT04316299 | 2/28/2020 | 2 | Completed | Observational | 287 | Acute Kidney Injury in Patients Hospitalized With COVID-19 | No Results Available | COVID-19|Acute Kidney Injury|Kidney Function | Rate of Acute Kidney Injury|Rate of Death|the length of hospital stay | Zhenhua Zen|Nanfang Hospital of Southern Medical University | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Retrospective | 3/8/2020 | 3/20/2020 | 2/26/2020 | 3/30/2020 | Hankou Hospital, Wuhan, Hubei, China | NCT04316299 | ||||||
11 | https://ClinicalTrials.gov/show/NCT04323332 | Phase 3 | 3/1/2020 | 0 | Not yet recruiting | Drug: Traditional Chinese Medicine Prescription | Interventional | 50 | Traditional Chinese Medicine for Severe COVID-19 | No Results Available | COVID-19 | Length of hospital stay (days)|Duration (days) of supplemental oxygenation|CT imaging changes|Mortality rate|Time to Clinical Improvement (TTCI)|The pneumonia severity index scores|Time to COVID-19 nucleic acid testing negativity in throat swab|Blood immune cell count|Serum inflammatory markers|Erythrocyte sedimentation rate|Platelet and D-dimer changes|Creatinine changes|Muscle enzymes changes|Usage of antibiotics|Usage of glucocorticoids|Frequency of adverse events | Xiyuan Hospital of China Academy of Chinese Medical Sciences | up to 85 Years (Child, Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 4/1/2020 | 3/26/2020 | 3/1/2020 | 3/26/2020 | Hao Li, Beijing, Beijing, China | NCT04323332 | ||||
12 | https://ClinicalTrials.gov/show/NCT04304313 | Phase 3 | 3/1/2020 | 21 | Recruiting | Drug: Sildenafil citrate tablets | Interventional | 10 | A Pilot Study of Sildenafil in COVID-19 | No Results Available | COVID-19 | Rate of disease remission|Rate of entering the critical stage|Time of entering the critical stage|Rate of no fever|Rate of respiratory symptom remission|Rate of lung imaging recovery|Rate of C-reactive protein (CRP) recovery|Rate of Biochemical criterion (CK, ALT, Mb) recovery|Rate of undetectable viral RNA (continuous twice)|Time for hospitalization|Rate of adverse event | Tongji Hospital | 18 Years and older (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 11/9/2020 | 3/11/2020 | 2/9/2020 | 3/17/2020 | Department and Institute of Infectious Disease, Wuhan, Hubei, China | NCT04304313 | ||||
13 | https://ClinicalTrials.gov/show/NCT04281693 | Not Applicable | 3/1/2020 | 29 | Not yet recruiting | Diagnostic Test: Standard screening strategy|Diagnostic Test: New screening strategy | Interventional | 230 | A New Screening Strategy for 2019 Novel Coronavirus Infection | No Results Available | Novel Coronavirus Infection Pneumonia | Screening accuracy|Cost-effectiveness analysis | Affiliated Hospital to Academy of Military Medical Sciences|The Fifth Medical Center of Chinese PLA General Hospital | Child, Adult, Older Adult | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Screening | 3/1/2020 | 2/24/2020 | 2/1/2020 | 2/24/2020 | the Fifth Medical Center of Chinese PLA General Hospital, Beijing, Beijing, China | NCT04281693 | ||||
14 | https://ClinicalTrials.gov/show/NCT04292964 | 3/13/2020 | 12 | Completed | Observational | 201 | Prognostic Factors of Patients With COVID-19 | No Results Available | SARS-CoV-2|Outcome, Fatal | all-cause mortality|Severe state | Chongqing Medical University | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 3/13/2020 | 3/3/2020 | 3/1/2020 | 3/17/2020 | The First Affiliated Hospital of Chongqing Medical University, Chongqing, China | NCT04292964 | ||||||
15 | https://ClinicalTrials.gov/show/NCT04312464 | 3/15/2020 | 74 | Enrolling by invitation | Other: non | Observational | 500 | Myocardial Damage in COVID-19 | No Results Available | COVID-19|Cardiovascular Diseases | The myocardial injury incidence|The risk factors analysis for the death|Clinical characteristics|Clinical course|Cardiovascular comorbidity|Analysis of causes of death | Wuhan Union Hospital, China | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Retrospective | 3/18/2020 | 3/18/2020 | 1/1/2020 | 3/18/2020 | Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China | NCT04312464 | |||||
16 | https://ClinicalTrials.gov/show/NCT04319315 | 3/16/2020 | 5 | Recruiting | Other: survey | Observational | 400 | Social Media Effect on Knowledge Dissemination During COVID-19 Virus Outbreak | No Results Available | COVID-19 | Number of physicians affected by social media measured by online survey designed to measure the influence of social media on medical practice | Assiut University | 25 Years to 65 Years (Adult, Older Adult) | Other | Observational Model: Other|Time Perspective: Prospective | 3/16/2020 | 3/24/2020 | 3/11/2020 | 3/24/2020 | Assiut University Hospitals, Assiut, Egypt | NCT04319315 | |||||
17 | https://ClinicalTrials.gov/show/NCT04320953 | Not Applicable | 3/16/2020 | 0 | Completed | Device: Non-contact MCE system | Interventional | 1 | Non-contact Endoscopy at Covid-19 Outbreak | No Results Available | Gastrointestinal Disease|Infectious Disease | Technical success|Clinical success|Adverse events | Changhai Hospital | 18 Years to 80 Years (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Other | 3/16/2020 | 3/25/2020 | 3/16/2020 | 3/25/2020 | Changhai Hospital, Shanghai, China | NCT04320953 | ||||
18 | https://ClinicalTrials.gov/show/NCT04306055 | Not Applicable | 3/19/2020 | 7 | Not yet recruiting | Other: Questionnaire with precaution information|Other: Experimental: Questionnaire without precaution information | Interventional | 1500 | Blood Donor Recruitment During Epidemic of COVID-19 | No Results Available | Blood Donation | Differences of attitude about blood donation towards different questionnaires|Rates of blood donation during 3 weeks | Guangzhou Blood Center | 18 Years to 60 Years (Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Health Services Research | 4/9/2020 | 3/12/2020 | 3/12/2020 | 3/12/2020 | NCT04306055 | |||||
19 | https://ClinicalTrials.gov/show/NCT04291729 | Phase 4 | 3/19/2020 | 31 | Completed | Drug: Ganovo+ritonavir+/-Interferon nebulization | Interventional | 11 | Evaluation of Ganovo (Danoprevir ) Combined With Ritonavir in the Treatment of Novel Coronavirus Infection | No Results Available | 2019-nCoV Pneumonia | Rate of composite adverse outcomes|Time to recovery|Rate of no fever|Rate of no cough|Rate of no dyspnea|Rate of no requiring supplemental oxygen|Rate of undetectable New coronavirus pathogen nucleic acid|Rate of mechanical ventilation|Rate of ICU admission|Rate of serious adverse event | The Ninth Hospital of Nanchang|Ascletis Pharmaceuticals Co., Ltd. | 18 Years to 75 Years (Adult, Older Adult) | Other|Industry | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 3/19/2020 | 3/2/2020 | 2/17/2020 | 3/24/2020 | The Ninth Hospital of Nanchang, Nanchang, Jiangxi, China | NCT04291729 | ||||
20 | https://ClinicalTrials.gov/show/NCT04321369 | 3/23/2020 | 14 | Completed | Diagnostic Test: Testing Sensitivity for SARS-CoV-2 Virus in Symptomatic Individuals | Observational | 533 | Impact of Swab Site and Sample Collector on Testing Sensitivity for SARS-CoV-2 Virus in Symptomatic Individuals | No Results Available | Infections, Respiratory|Fever|Cough | Accuracy of patient administered tests | Dr. Deneen Vojta|Quest Diagnostics|Bill and Melinda Gates Foundation|UnitedHealth Group | Child, Adult, Older Adult | Industry|Other | Observational Model: Case-Only|Time Perspective: Retrospective | 3/23/2020 | 3/25/2020 | 3/9/2020 | 3/25/2020 | Everett Clinic, Seattle, Washington, United States | NCT04321369 | |||||
21 | https://ClinicalTrials.gov/show/NCT04318301 | 3/28/2020 | 7 | Active, not recruiting | Observational | 275 | Hypertension in Patients Hospitalized With COVID-19 | HT-COVID19 | No Results Available | COVID-19|Hypertension | Rate of Death|the severity of pneumonia | Zhenhua Zen|Nanfang Hospital of Southern Medical University | 18 Years to 100 Years (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Retrospective | 3/30/2020 | 3/23/2020 | 3/21/2020 | 3/24/2020 | Hankou Hospital, Hankou, Hubei, China | NCT04318301 | |||||
22 | https://ClinicalTrials.gov/show/NCT04272710 | 3/31/2020 | 66 | Withdrawn | Observational | 0 | Prognositc Factors in COVID-19 Patients Complicated With Hypertension | No Results Available | 2019-nCoV | Occupancy rate in the intensive care unit (ICU)|Mechanical Ventilation|Death|All cause mortality|Time from onset of symptoms to main outcome and its components|Time to Clinical Recovery | Chongqing Medical University | 18 Years to 100 Years (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 4/30/2020 | 2/17/2020 | 1/25/2020 | 3/17/2020 | The First Affiliated Hospital of Chongqing Medical University, Chongqing, China | NCT04272710 | ||||||
23 | https://ClinicalTrials.gov/show/NCT04280913 | 3/31/2020 | 38 | Withdrawn | Other: retrospective analysis | Observational | 0 | Clinical Outcomes of Patients With COVID19 | No Results Available | Coronavirus Disease 2019 | Time to negative conversion of severe acute respiratory syndrome coronavirus 2|Length of stay in hospital|Survival|Intubation | Guangzhou Institute of Respiratory Disease|Huizhou Municipal Central Hospital | Child, Adult, Older Adult | Other | Observational Model: Cohort|Time Perspective: Retrospective | 3/31/2020 | 2/21/2020 | 2/22/2020 | 3/19/2020 | HuiZhou Municipal Central Hospital, Huizhou, Guangdong, China | NCT04280913 | |||||
24 | https://ClinicalTrials.gov/show/NCT04287686 | Not Applicable | 4/1/2020 | 60 | Withdrawn | Drug: Recombinant human angiotensin-converting enzyme 2 (rhACE2) | Interventional | 0 | Recombinant Human Angiotensin-converting Enzyme 2 (rhACE2) as a Treatment for Patients With COVID-19 | No Results Available | COVID-19 | Time course of body temperature (fever)|Viral load over time|P/F ratio over time|Sequential organ failure assessment score(SOFA score) over time|Pulmonary Severity Index (PSI)|Image examination of chest over time|Proportion of subjects who progressed to critical illness or death|Time from first dose to conversion to normal or mild pneumonia|T-lymphocyte counts over time|C-reactive protein levels over time|Angiotensin II (Ang II) changes over time|Angiotensin 1-7 (Ang 1-7) changes over time|Angiotensin 1-5 (Ang 1-5) changes over time|Renin changes over time|Aldosterone changes over time|Angiotensin-converting enzyme (ACE) changes over time|Angiotensin-converting enzyme 2 (ACE2) changes over time|Interleukin 6 (IL-6) changes over time|Interleukin 8 (IL-8) changes over time|Soluble tumor necrosis factor receptor type II (sTNFrII) changes over time|Plasminogen activator inhibitor type-1 (PAI-1) changes over time|Von willebrand factor (vWF) changes over time|Tumor necrosis factor-α (TNF-α) changes over time|Soluble receptor for advanced glycation end products (sRAGE) changes over time|Surfactant protein-D (SP-D) changes over time|Angiopoietin-2 changes over time|Frequency of adverse events and severe adverse events | The First Affiliated Hospital of Guangzhou Medical University | 18 Years to 80 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 4/1/2020 | 2/27/2020 | 2/1/2020 | 3/17/2020 | GCP Office of The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China | NCT04287686 | ||||
25 | https://ClinicalTrials.gov/show/NCT04275414 | Phase 2|Phase 3 | 4/1/2020 | 60 | Recruiting | Drug: Bevacizumab Injection | Interventional | 20 | Bevacizumab in Severe or Critical Patients With COVID-19 Pneumonia | BEST-CP | No Results Available | Coronavirus Infections | Partial arterial oxygen pressure (PaO2) to fraction of inspiration O2 (FiO2) ratio|Degree of dyspnea (Liker scale)|Degree of dyspnea (VAS)|The area of lung lesions on Chest CT|The degree of lung exudation on Chest CT|SpO2|PaO2|CRP|hs-CRP|All-cause mortality | Qilu Hospital of Shandong University | 18 Years to 80 Years (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 2/19/2020 | 2/1/2020 | 2/19/2020 | Qilu Hospital of Shandong University, Jinan, Shandong, China | NCT04275414 | |||
26 | https://ClinicalTrials.gov/show/NCT04315480 | Phase 2 | 4/1/2020 | 31 | Not yet recruiting | Drug: Tocilizumab | Interventional | 30 | Tocilizumab for SARS-CoV2 Severe Pneumonitis | No Results Available | SARS Pneumonia | arrest in deterioration of pulmonary function|improving in pulmonary function|need of oro-tracheal intubation|death | Università Politecnica delle Marche|Azienda Ospedaliera Ospedali Riuniti Marche Nord | 18 Years to 90 Years (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 3/19/2020 | 3/1/2020 | 3/19/2020 | Università Politecnica delle Marche, Ancona, AN, Italy | "Study Protocol", https://ClinicalTrials.gov/ProvidedDocs/80/NCT04315480/Prot_000.pdf | NCT04315480 | |||
27 | https://ClinicalTrials.gov/show/NCT04328454 | 4/2/2020 | 63 | Recruiting | Other: retrospective analysis | Observational | 120 | Clinical Characteristics and Prognostic Factors of Patients With COVID-19 | No Results Available | Coronavirus | Time to negative conversion of severe acute respiratory syndrome coronavirus 2|Length of stay in hospital|Survival|Intubation | Shanghai 10th People's Hospital|Chibi People's Hospital, Hubei Province | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 4/15/2020 | 3/31/2020 | 1/30/2020 | 3/31/2020 | Shanghai 10th People's Hospital, Shanghai, Shanghai, China | NCT04328454 | |||||
28 | https://ClinicalTrials.gov/show/NCT04257656 | Phase 3 | 4/3/2020 | 57 | Recruiting | Drug: Remdesivir|Drug: Remdesivir placebo | Interventional | 453 | Severe 2019-nCoV Remdesivir RCT | No Results Available | 2019-nCov|Remdesivir | Time to Clinical Improvement (TTCI) [Censored at Day 28]|Clinical status|Time to Hospital Discharge OR NEWS2 (National Early Warning Score 2) of ≤ 2 maintained for 24 hours.|All cause mortality|Duration (days) of mechanical ventilation|Duration (days) of extracorporeal membrane oxygenation|Duration (days) of supplemental oxygenation|Length of hospital stay (days)|Time to 2019-nCoV RT-PCR negativity in upper and lower respiratory tract specimens|Change (reduction) in 2019-nCoV viral load in upper and lower respiratory tract specimens as assessed by area under viral load curve.|Frequency of serious adverse drug events | Capital Medical University | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 5/1/2020 | 2/6/2020 | 2/6/2020 | 2/24/2020 | Bin Cao, Beijing, Beijing, China | NCT04257656 | ||||
29 | https://ClinicalTrials.gov/show/NCT04327804 | 4/3/2020 | 9 | Recruiting | Diagnostic Test: Odd/Even birth year intervention groups | Observational | 120 | A Longitudinal Study of SARS-CoV-2 Positive Patients Testing Nasal Swabs and Collecting Blood Samples for Research | No Results Available | SARS-CoV Infection | Detection of SARS-CoV-2 virus|Trajectory of COVID-19 and antibody development | Dr. Deneen Vojta|PATH|Mayo Clinic|Bill and Melinda Gates Foundation|UnitedHealth Group | Child, Adult, Older Adult | Industry|Other | Observational Model: Case-Only|Time Perspective: Prospective | 4/10/2020 | 3/31/2020 | 3/25/2020 | 3/31/2020 | Everett Clinic, Seattle, Washington, United States | NCT04327804 | |||||
30 | https://ClinicalTrials.gov/show/NCT04318418 | 4/10/2020 | 18 | Not yet recruiting | Observational | 5000 | ACE Inhibitors, Angiotensin II Type-I Receptor Blockers and Severity of COVID-19 | CODIV-ACE | No Results Available | COVID-19 | Severe COVID-19|Death | Neuromed IRCCS | Child, Adult, Older Adult | Other | Observational Model: Case-Control|Time Perspective: Retrospective | 4/30/2020 | 3/24/2020 | 3/23/2020 | 3/24/2020 | IRCCS Neuromed, Department of Epidemiology and Prevention, Pozzilli, Italy | NCT04318418 | |||||
31 | https://ClinicalTrials.gov/show/NCT04252664 | Phase 3 | 4/10/2020 | 58 | Recruiting | Drug: Remdesivir|Drug: Remdesivir placebo | Interventional | 308 | Mild/Moderate 2019-nCoV Remdesivir RCT | No Results Available | 2019-nCoV | Time to Clinical recoveryTime to Clinical Recovery (TTCR)|All cause mortality|Frequency of respiratory progression|Time to defervescence (in those with fever at enrolment)|Time to cough reported as mild or absent (in those with cough at enrolment rated severe or moderate)|Time to dyspnea reported as mild or absent (on a scale of severe, moderate, mild absent, in those with dyspnoea at enrolment rated as severe or moderate,)|Frequency of requirement for supplemental oxygen or non-invasive ventilation|Time to 2019-nCoV RT-PCR negative in upper respiratory tract specimen|Change (reduction) in 2019-nCoV viral load in upper respiratory tract specimen as assessed by area under viral load curve.|Frequency of requirement for mechanical ventilation|Frequency of serious adverse events | Capital Medical University|Chinese Academy of Medical Sciences | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 4/27/2020 | 2/5/2020 | 2/12/2020 | 2/24/2020 | Jin Yin-tan hospital, Wu Han, Hubei, China | NCT04252664 | ||||
32 | https://ClinicalTrials.gov/show/NCT04324736 | 4/10/2020 | 11 | Not yet recruiting | Other: no interventional study | Observational | 300 | "Coronavirus SARS-CoV2 and Diabetes Outcomes" | CORONADO | No Results Available | Coronavirus|Diabetes | Assess the prevalence of severe forms among hospitalized patients with diabètes and COVID-19|describe the clinical and biological characteristics of hospitalized subjects with diabetes and COVID-19|describe the prognosis of hospitalized subjects with diabetes and COVID-19|describe the care management of hospitalized subjects with diabetes and COVID-19 | Nantes University Hospital | Child, Adult, Older Adult | Other | Observational Model: Cohort|Time Perspective: Other | 5/8/2020 | 3/27/2020 | 3/30/2020 | 3/31/2020 | NCT04324736 | |||||
33 | https://ClinicalTrials.gov/show/NCT04273763 | Not Applicable | 4/15/2020 | 59 | Enrolling by invitation | Drug: Bromhexine Hydrochloride Tablets|Drug: Arbidol Hydrochloride Granules|Drug: Recombinant Human Interferon α2b Spray | Interventional | 60 | Evaluating the Efficacy and Safety of Bromhexine Hydrochloride Tablets Combined With Standard Treatment/ Standard Treatment in Patients With Suspected and Mild Novel Coronavirus Pneumonia (COVID-19) | No Results Available | Novel Coronavirus Pneumonia|2019-nCoV | Time to clinical recovery after treatment|Rate of aggravation|Clinical remission rate|Dynamic changes of oxygenation index|Time to cure|rate to cure|Time to defervescence|Time to cough remission|Time to dyspnea remission|Days of supplemental oxygenation|Rate of patients with requring supplemental oxygen|Rate of patients with mechanical ventilation|Time of negative COVID-19 nucleic acid results|Rate of negative COVID-19 nucleic acid results|Rate of ICU admission|28-day mortality | Second Affiliated Hospital of Wenzhou Medical University|WanBangDe Pharmaceutical Group Co.,Ltd. | 18 Years to 80 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Sequential Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 4/30/2020 | 2/18/2020 | 2/16/2020 | 3/23/2020 | The Second AffIliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China | NCT04273763 | ||||
34 | https://ClinicalTrials.gov/show/NCT04260308 | 4/15/2020 | 72 | Recruiting | Observational | 30000 | A Survey of Psychological Status of Medical Workers and Residents in the Context of 2019 Novel Coronavirus Pneumonia | No Results Available | Virus; Pneumonia | GHQ-12(general health questionnaire-12)|IES-R(Impact of Event Scale-Revised) | Huazhong University of Science and Technology | Child, Adult, Older Adult | Other | Observational Model: Case-Only|Time Perspective: Prospective | 4/20/2020 | 2/7/2020 | 2/3/2020 | 2/7/2020 | Tongji Hospital,Tongji Medical College Affiliated,Huazhong University of Science & Technology, Wuhan, Hubei, China | NCT04260308 | ||||||
35 | https://ClinicalTrials.gov/show/NCT04307459 | 4/19/2020 | 31 | Not yet recruiting | Other: standard operating procedures | Observational | 50 | Acute Respiratory Failure and Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection in Real Life | No Results Available | Coronavirus Infections|Respiratory Failure|Ventilator Lung | Real life data of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection|in-hospital mortality|30 days mortality|6 months mortality|Intubation rate|Time to Intubation|Time to ventilation|Non invasive to Invasive time|Recovery rate|Recurrence rate|Risk factor for COVID19|Blood tests and outcome|Antiviral therapy|Coinfections|Radiological findings|Ultrasound findings|Myocardial injury|Medical management | University of Milan | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Prospective | 12/31/2020 | 3/13/2020 | 3/19/2020 | 3/17/2020 | Luigi Sacco University Hospital, Milan, Lombardia, Italy | NCT04307459 | |||||
36 | https://ClinicalTrials.gov/show/NCT04315870 | 4/20/2020 | 110 | Recruiting | Other: pregnant women with laboratory-confirmed 2019-n-CoV | Observational | 20 | Clinical Characteristics of Coronavirus Disease 2019 (COVID-19) in Pregnancy: The Italian Registry on Coronavirus in Pregnancy. | I-COVID | No Results Available | Infection Viral | Maternal and perinatal outcomes | Federico II University | 18 Years to 50 Years (Adult) | Other | Observational Model: Cohort|Time Perspective: Other | 4/30/2020 | 3/20/2020 | 1/1/2020 | 3/20/2020 | University of Naples Federico II, Napoli, Italy | NCT04315870 | ||||
37 | https://ClinicalTrials.gov/show/NCT04308668 | Phase 3 | 4/21/2020 | 35 | Recruiting | Drug: Hydroxychloroquine|Other: Placebo | Interventional | 3000 | Post-exposure Prophylaxis / Preemptive Therapy for SARS-Coronavirus-2 | COVID-19 PEP | No Results Available | Corona Virus Infection|Acute Respiratory Distress Syndrome|SARS-CoV Infection|Coronavirus|Coronavirus Infections | Incidence of COVID19 Disease among those who are asymptomatic at trial entry|Ordinal Scale of COVID19 Disease Severity at 14 days among those who are symptomatic at trial entry|Incidence of Hospitalization|Incidence of Death|Incidence of Confirmed SARS-CoV-2 Detection|Incidence of Symptoms Compatible with COVID19 (possible disease)|Incidence of All-Cause Study Medicine Discontinuation or Withdrawal|Overall symptom severity at 5 and 14 day | University of Minnesota | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 5/12/2020 | 3/16/2020 | 3/17/2020 | 3/27/2020 | Nationwide Enrollment via Internet, please email: covid19@umn.edu, Minneapolis, Minnesota, United States|University of Minnesota, Minneapolis, Minnesota, United States|Internet, New York, New York, United States | NCT04308668 | |||
38 | https://ClinicalTrials.gov/show/NCT04324489 | Not Applicable | 4/25/2020 | 50 | Recruiting | Drug: DAS181 | Interventional | 4 | DAS181 for COVID-19: Compassionate Use | No Results Available | COVID-19 | Improved clinical status|Return to room air|SARS-CoV-2 RNA|Discharge|Death | Renmin Hospital of Wuhan University|Ansun Biopharma, Inc. | 18 Years to 70 Years (Adult, Older Adult) | Other|Industry | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 4/30/2020 | 3/27/2020 | 3/6/2020 | 3/27/2020 | Renmin Hospital of Wuhan University, Wuhan, Hubei, China | NCT04324489 | ||||
39 | https://ClinicalTrials.gov/show/NCT04323345 | Phase 3 | 4/25/2020 | 31 | Not yet recruiting | Dietary Supplement: Natural Honey|Other: Standard Care | Interventional | 1000 | Efficacy of Natural Honey Treatment in Patients With Novel Coronavirus | No Results Available | COVID-19 | Rate of recovery from positive to negative swaps|Fever to normal temperature in days|Resolution of lung inflammation in CT or X ray|30 days mortality rate|Number of days till reaching negative swab results | Misr University for Science and Technology | 5 Years to 75 Years (Child, Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Investigator)|Primary Purpose: Treatment | 5/10/2020 | 3/26/2020 | 3/25/2020 | 3/26/2020 | Mahmoud Tantawy, Cairo, Egypt | NCT04323345 | ||||
40 | https://ClinicalTrials.gov/show/NCT04244591 | Phase 2|Phase 3 | 4/25/2020 | 90 | Recruiting | Drug: methylprednisolone therapy|Other: Standard care | Interventional | 80 | Glucocorticoid Therapy for Novel CoronavirusCritically Ill Patients With Severe Acute Respiratory Failure | Steroids-SARI | No Results Available | Coronavirus Infections|Respiratory Infection Virus | Lower Murray lung injury score|The difference of PaO2/FiO2 between two groups|Lower Sequential Organ Failure Assessment (SOFA) score|Mechanical ventilation support|Clearance of noval coronavirus|All-cause mortality | Peking Union Medical College Hospital|Zhongda Hospital|Zhongnan Hospital|Renmin Hospital of Wuhan University | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 12/25/2020 | 1/28/2020 | 1/26/2020 | 2/13/2020 | Medical ICU,Peking Union Medical College Hospital, Beijing, Beijing, China | NCT04244591 | |||
41 | https://ClinicalTrials.gov/show/NCT04327531 | 4/26/2020 | 31 | Active, not recruiting | Behavioral: turkish physicians | Observational | 200 | Evaluation of Covid 19 Knowledge Anxiety and Expectation Levels of Turkish Physicians, Survey Study | No Results Available | COVID-19|Physician-Patient Relations | Evaluation of covid-19 knowledge level of turkish physicians | Kanuni Sultan Suleyman Training and Research Hospital | 25 Years to 55 Years (Adult) | Other | Observational Model: Ecologic or Community|Time Perspective: Prospective | 4/28/2020 | 3/31/2020 | 3/26/2020 | 3/31/2020 | Pinar Yalcin Bahat, Istanbul, İ̇stanbul, Turkey | NCT04327531 | |||||
42 | https://ClinicalTrials.gov/show/NCT04275947 | 4/30/2020 | 76 | Recruiting | Other: nCapp, a cell phone-based auto-diagnosis system | Observational | 450 | The COVID-19 Mobile Health Study (CMHS) | CMHS | No Results Available | COVID-19 | Accuracy of nCapp COVID-19 risk diagnostic model | Chinese Alliance Against Lung Cancer|Shanghai Respiratory Research Institution | 18 Years to 90 Years (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Prospective | 5/31/2020 | 2/19/2020 | 2/14/2020 | 2/19/2020 | Renmin Hospital of Wuhan University, Wuhan, Hubei, China | NCT04275947 | ||||
43 | https://ClinicalTrials.gov/show/NCT04273581 | Phase 2 | 4/30/2020 | 72 | Not yet recruiting | Drug: placebo|Drug: Thalidomide | Interventional | 40 | The Efficacy and Safety of Thalidomide Combined With Low-dose Hormones in the Treatment of Severe COVID-19 | No Results Available | COVID-19 Thalidomide | Time to Clinical Improvement (TTCI)|Clinical status|Time to Hospital Discharge OR NEWS2 (National Early Warning Score 2) of ≤ 2 maintained for 24 hours|All cause mortality|Duration (days) of mechanical ventilation|Duration (days) of extracorporeal membrane oxygenation|Duration (days) of supplemental oxygenation|Length of hospital stay (days)|Time to 2019-nCoV RT-PCR negativity in upper and lower respiratory tract specimens|Change (reduction) in 2019-nCoV viral load in upper and lower respiratory tract specimens as assessed by area under viral load curve.|Frequency of serious adverse drug events|Serum TNF-α, IL-1β, IL-2, IL-6, IL-7, IL-10, GSCF, IP10#MCP1, MIP1α and other cytokine expression levels before and after treatment | First Affiliated Hospital of Wenzhou Medical University|Second Affiliated Hospital of Wenzhou Medical University|Wenzhou Central Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 5/30/2020 | 2/18/2020 | 2/18/2020 | 2/21/2020 | NCT04273581 | |||||
44 | https://ClinicalTrials.gov/show/NCT04251767 | Not Applicable | 4/30/2020 | 85 | Withdrawn | Other: washed microbiota transplantation|Other: placebo | Interventional | 0 | Washed Microbiota Transplantation for Patients With 2019-nCoV Infection | No Results Available | COVID-19 Complicated With Refractory Intestinal Infections | Number of participants with improvement from severe type to common type | The Second Hospital of Nanjing Medical University | 14 Years to 70 Years (Child, Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 4/30/2020 | 2/5/2020 | 2/5/2020 | 3/17/2020 | Medical Center for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China | NCT04251767 | ||||
45 | https://ClinicalTrials.gov/show/NCT04268537 | Phase 2 | 4/30/2020 | 80 | Not yet recruiting | Drug: PD-1 blocking antibody+standard treatment|Drug: Thymosin+standard treatment|Other: standard treatment | Interventional | 120 | Immunoregulatory Therapy for 2019-nCoV | No Results Available | 2019 nCoV, PD-1 | lung injury score|absolute lymphocyte counts|serum level of CRP, PCT and IL-6|SOFA score|all cause mortality rate|ventilation free days|ICU free days | Southeast University, China | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 10/31/2020 | 2/13/2020 | 2/10/2020 | 2/13/2020 | NCT04268537 | |||||
46 | https://ClinicalTrials.gov/show/NCT04261426 | Phase 2|Phase 3 | 4/30/2020 | 80 | Not yet recruiting | Drug: Intravenous Immunoglobulin|Other: Standard care | Interventional | 80 | The Efficacy of Intravenous Immunoglobulin Therapy for Severe 2019-nCoV Infected Pneumonia | No Results Available | 2019-nCoV | Clinical improvement based on the 7-point scale|Lower Murray lung injury score|28-day mortality|Duration of mechanical ventilation|Duration of hospitalization|Proportion of patients with negative RT-PCR results|Proportion of patients in each category of the 7-point scale|Proportion of patients with normalized inflammation factors|Frequency of Adverse Drug Events|Frequency of Serious Adverse Drug Events | Peking Union Medical College Hospital|Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 2/7/2020 | 2/10/2020 | 2/7/2020 | NCT04261426 | |||||
47 | https://ClinicalTrials.gov/show/NCT04316949 | 4/30/2020 | 41 | Recruiting | Observational | 350 | Predictors of Respiratory Failure in SARS-Cov-2 Infection | No Results Available | SARS-CoV-2 Pneumonia | Respiratory failure|Occurence of bacterial superinfection | University of Bologna | 18 Years to 99 Years (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 5/31/2020 | 3/20/2020 | 3/20/2020 | 3/27/2020 | University of Bologna - Department of Medical and Surgical Sciences, Bologna, Italy | NCT04316949 | ||||||
48 | https://ClinicalTrials.gov/show/NCT04320277 | Phase 3 | 4/30/2020 | 45 | Recruiting | Drug: Baricitinib | Interventional | 60 | Baricitinib in Symptomatic Patients Infected by COVID-19: an Open-label, Pilot Study. | BARI-COVID | No Results Available | Pharmacological Action | The percentage of patients requiring transfer to ICU as compared with the rate of transfers observed in controls.|The percentage of patients achieving the remission; CRP, IL-6 and TNFα values at baseline and during the treatment course; the number of AEs. | Hospital of Prato | 18 Years to 85 Years (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Crossover Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 4/30/2020 | 3/24/2020 | 3/16/2020 | 3/24/2020 | Fabrizio Cantini, Prato, Tuscany, Italy | NCT04320277 | |||
49 | https://ClinicalTrials.gov/show/NCT04264858 | Not Applicable | 4/30/2020 | 44 | Not yet recruiting | Drug: Immunoglobulin of cured patients|Drug: γ-Globulin | Interventional | 10 | Treatment of Acute Severe 2019-nCoV Pneumonia With Immunoglobulin From Cured Patients | No Results Available | 2019-nCoV|Immunoglobulin of Cured Patients | Time to Clinical Improvement (TTCI)|Clinical status assessed by the ordinal scale|The differences in oxygen intake methods|Duration (days) of supplemental oxygenation|Duration (days) of mechanical ventilation|The mean PaO2/FiO2|The lesions of the pulmonary segment numbers involved in pulmonary CT [ every 7 days]|Time to 2019-nCoV RT-PCR negativity in respiratory tract specimens [every 3 days]|Dynamic changes of 2019-nCoV antibody titer in blood|Length of hospital stay (days)|All cause mortality | Wuhan Union Hospital, China | 18 Years and older (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/31/2020 | 2/11/2020 | 3/17/2020 | 3/17/2020 | Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China | NCT04264858 | ||||
50 | https://ClinicalTrials.gov/show/NCT04319016 | 4/30/2020 | 120 | Recruiting | Other: pregnant women with laboratory-confirmed 2019-n-CoV | Observational | 20 | Clinical Characteristics of Coronavirus Disease 2019 (COVID-19) in Pregnancy | COVID-preg | No Results Available | Infection Viral | Maternal and perinatal outcomes | Federico II University | Child, Adult, Older Adult | Other | Observational Model: Cohort|Time Perspective: Other | 5/1/2020 | 3/24/2020 | 1/1/2020 | 3/24/2020 | Gabriele Saccone, Napoli, Italy | NCT04319016 | ||||
51 | https://ClinicalTrials.gov/show/NCT04292327 | 4/30/2020 | 120 | Active, not recruiting | Observational | 400 | Clinical Progressive Characteristics and Treatment Effects of 2019-novel Coronavirus | 2019-nCoV | No Results Available | Pneumonia Caused by Human Coronavirus | Mortality|The time interval of Nucleic acid detection become negative | Fujian Provincial Hospital | 18 Years to 75 Years (Adult, Older Adult) | Other | Observational Model: Other|Time Perspective: Retrospective | 7/31/2020 | 3/3/2020 | 1/1/2020 | 3/3/2020 | Fujian Provincial Hospital, Fuzhou, Fujian, China | NCT04292327 | |||||
52 | https://ClinicalTrials.gov/show/NCT04269525 | Phase 2 | 4/30/2020 | 84 | Recruiting | Biological: UC-MSCs | Interventional | 10 | Umbilical Cord(UC)-Derived Mesenchymal Stem Cells(MSCs) Treatment for the 2019-novel Coronavirus(nCOV) Pneumonia | No Results Available | Pneumonia, Viral|Pneumonia, Ventilator-Associated | Oxygenation index|28 day mortality|Hospital stay|2019-nCoV nucleic acid test|Improvement of lung imaging examinations|White blood cell count|Lymphocyte count|Lymphocyte percentage|Procalcitonin|interleukin(IL)-2|IL-4|IL-6|IL-8|IL-10|tumor necrosis factor(TNF)-α|γ-interferon(IFN) | ZhiYong Peng|Tuohua Biological Technology Co. Ltd|Zhongnan Hospital | 18 Years to 75 Years (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Prevention | 9/30/2020 | 2/13/2020 | 2/6/2020 | 2/17/2020 | Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China | NCT04269525 | ||||
53 | https://ClinicalTrials.gov/show/NCT04061382 | 4/30/2020 | 198 | Recruiting | Procedure: venepuncture | Observational | 2300 | Sero-epidemiological Survey of England in 2019/2020 | STORY | No Results Available | Serogroup C Meningococcal Meningitis|Diphtheria|COVID-19 | Feasibility of developing a UK based sero-epidemiological programme in 0-24 year olds|Feasibility of developing a UK based sero epidemiological survey in 0-24 year olds|Recruitment rate|Cost|To assess, in relevant age groups, immunity against infections and vaccine preventable diseases|Sera collection | University of Oxford | up to 24 Years (Child, Adult) | Other | Observational Model: Other|Time Perspective: Prospective | 11/30/2020 | 8/19/2019 | 10/15/2019 | 3/24/2020 | Centre for Clinical Vaccinology & Tropical Medicine (CCVTM), Oxford, Oxfordshire, United Kingdom | NCT04061382 | ||||
54 | https://ClinicalTrials.gov/show/NCT04255940 | 4/30/2020 | 101 | Recruiting | Observational | 12000 | 2019-nCoV Outbreak and Cardiovascular Diseases | No Results Available | Cardiovascular Death; Major Adverse Cardiovascular Events | Cardiovascular Death|Major Adverse Cardiovascular Events|Times From symptom onset to hospital arrival|Anxiety | Qilu Hospital of Shandong University | Child, Adult, Older Adult | Other | Observational Model: Case-Only|Time Perspective: Prospective | 4/30/2020 | 2/5/2020 | 1/20/2020 | 2/5/2020 | Affiliated Hospital of Binzhou Medical Universty, Binzhou, Shandong, China|Heze Municipal Hospital, Heze, Shandong, China|Shandong University Qilu Hospital, Jinan, Shandong, China|Jinan Central Hospital, Shandong University, Jinan, Shandong, China|First Hospital Affiliated with Shandong First Medical University, Jinan, Shandong, China|Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China|The Second Hospital of Shandong University, Jinan, Shandong, China|Jining Hospital of Traditional Chinese Medicine, Jining, Shandong, China|Qihe People's Hospital, Qihe, Shandong, China|Affiliated Hospital of Qingdao University Medical College, Qingdao, Shandong, China|Weihai Municipal Hospital, Weihai, Shandong, China|Central Hospital of Zibo, Zibo, Shandong, China | NCT04255940 | ||||||
55 | https://ClinicalTrials.gov/show/NCT04306497 | 5/1/2020 | 60 | Recruiting | Drug: TCM prescriptions | Observational | 340 | Clinical Trial on Regularity of TCM Syndrome and Differentiation Treatment of COVID-19. | CTOROTSADTOC | No Results Available | COVID-19 | The relief / disappearance rate of main symptoms|Chest CT absorption|Virus antigen negative conversion rate|Clinical effective time: the average effective time|The number of severe and critical conversion cases|Incidence of complications|Traditional Chinese Medicine Syndrome Score | Jiangsu Famous Medical Technology Co., Ltd. | 18 Years to 75 Years (Adult, Older Adult) | Industry | Observational Model: Cohort|Time Perspective: Prospective | 5/1/2020 | 3/13/2020 | 3/2/2020 | 3/17/2020 | Huai'an fourth people's Hospital, Huaian, Jiangsu, China | NCT04306497 | ||||
56 | https://ClinicalTrials.gov/show/NCT04307693 | Phase 2 | 5/1/2020 | 51 | Recruiting | Drug: Lopinavir/ritonavir|Drug: Hydroxychloroquine sulfate | Interventional | 150 | Comparison of Lopinavir/Ritonavir or Hydroxychloroquine in Patients With Mild Coronavirus Disease (COVID-19) | No Results Available | COVID-19 | Viral load|Viral load change|Time to clinical improvement (TTCI)|Percentage of progression to supplemental oxygen requirement by day 7|Time to NEWS2 (National Early Warning Score 2) of 3 or more maintained for 24 hours by day 7|Time to clinical failure, defined as the time to death, mechanical ventilation, or ICU admission|Rate of switch to Lopinavir/ritonavir or hydroxychloroquine by day 7|adverse effects|Concentration of Lopinavir/ritonavir and hydroxychloroquine | Asan Medical Center | 16 Years to 99 Years (Child, Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 3/13/2020 | 3/11/2020 | 3/13/2020 | Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea, Republic of | NCT04307693 | ||||
57 | https://ClinicalTrials.gov/show/NCT04292899 | Phase 3 | 5/1/2020 | 56 | Recruiting | Drug: Remdesivir|Drug: Standard of Care | Interventional | 400 | Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Severe Coronavirus Disease (COVID-19) | No Results Available | COVID-19 | Proportion of Participants With Normalization of Fever and Oxygen Saturation Through Day 14|Proportion of Participants With Treatment Emergent Adverse Events Leading to Study Drug Discontinuation | Gilead Sciences | 18 Years and older (Adult, Older Adult) | Industry | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 3/3/2020 | 3/6/2020 | 3/31/2020 | Kaiser Permanente Los Angeles Medical Center, Los Angeles, California, United States|Hoag Memorial Hospital Presbyterian, Newport Beach, California, United States|Providence St. Johns Medical Center, Santa Monica, California, United States|Stanford Hospital, Stanford, California, United States|University of Chicago, Chicago, Illinois, United States|Brigham & Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States|Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States|Hackensack University Medical Center, Hackensack, New Jersey, United States|Jamaica Hospital Medical Center, Jamaica, New York, United States|Danbury Hospital, Lagrangeville, New York, United States|New York Presbyterian Hospital/Weill Cornell Medical College, New York, New York, United States|Providence Portland Medical Center, Portland, Oregon, United States|Providence St. Vincent Medical Center, Portland, Oregon, United States|The Miriam Hospital, Providence, Rhode Island, United States|Baylor University Medical Center, Dallas, Texas, United States|Houston Methodist Hospital, Houston, Texas, United States|VCU Health Medical Center, Richmond, Virginia, United States|Providence Regional Medical Center Everett, Everett, Washington, United States|Swedish Center for Comprehensive Care, Seattle, Washington, United States|MultiCare Deaconess Hospital, Spokane, Washington, United States|MultiCare Tacoma General Hospital, Tacoma, Washington, United States|Klinikum rechts der Isar der TU Munchen, Klinik und Poliklinik Innere Medizin 2, Munich, Germany|Prince of Wales Hospital, Hong Kong, Hong Kong|Princess Margaret Hospital, Hong Kong, Hong Kong|Queen Mary Hospital, Hong Kong, Hong Kong|ASST degli Spedali Civili di Brescia - Spedali Civ, Brescia, Italy|ASST di Cremona - Azienda Socio Sanitaria Territor, Cremona, Italy|UOC Medicina Di Laboratorio, Azienda Ospedaliera di Padova, Padova PD, Italy|Azienda Ospedaliero Universitaria di Parma, Parma, Italy|UOC Malattie Infettive I, Fondazione IRCCS Policlinio San Matteo, Pavia, Italy|Kyungpook National University Hospital, Daegu, Korea, Republic of|Seoul Medical Center, Seoul, Korea, Republic of|National Medical Center, Seoul, Korea, Republic of|National University Hospital, Singapore, Singapore|Singapore General Hospital, Singapore, Singapore|National Centre for Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore|Hospital Clinic de Barcelona, Barcelona, Spain|Hospital Universitario La Paz, Madrid, Spain|Hopitaux Universitaires de Genève, Genève 14, Switzerland|Ospedale Regionale di Locarno La Carità, Lugano, Switzerland|Universitätsspital Zürich, Zürich, Switzerland|Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan|China Medical University Hospital, Taichung, Taiwan|National Taiwan University Hospital, Taipei City, Taiwan | NCT04292899 | ||||
58 | https://ClinicalTrials.gov/show/NCT04292730 | Phase 3 | 5/1/2020 | 47 | Recruiting | Drug: Remdesivir|Drug: Standard of Care | Interventional | 600 | Study to Evaluate the Safety and Antiviral Activity of Remdesivir (GS-5734™) in Participants With Moderate Coronavirus Disease (COVID-19) Compared to Standard of Care Treatment | No Results Available | COVID-19 | Proportion of Participants Discharged by Day 14|Proportion of Participants With Treatment Emergent Adverse Events Leading to Study Drug Discontinuation | Gilead Sciences | 18 Years and older (Adult, Older Adult) | Industry | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 3/3/2020 | 3/15/2020 | 3/31/2020 | Kaiser Permanente Los Angeles Medical Center, Los Angeles, California, United States|Hoag Memorial Hospital Presbyterian, Newport Beach, California, United States|Stanford Hospital, Stanford, California, United States|University of Chicago, Chicago, Illinois, United States|Brigham & Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States|Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States|Jamaica Hospital Medical Center, Jamaica, New York, United States|Danbury Hospital, Lagrangeville, New York, United States|Providence Portland Medical Center, Portland, Oregon, United States|Providence St. Vincent Medical Center, Portland, Oregon, United States|The Miriam Hospital, Providence, Rhode Island, United States|Baylor University Medical Center, Dallas, Texas, United States|Houston Methodist Hospital, Houston, Texas, United States|Providence Medical Research Center, Everett, Washington, United States|Swedish Center for Comprehensive Care, Seattle, Washington, United States|MultiCare Tacoma General Hospital, Tacoma, Washington, United States|Klinikum rechts der Isar der TU Munchen, Klinik und Poliklinik Innere Medizin 2, Munich, Germany|Prince of Wales Hospital, Hong Kong, Hong Kong|Princess Margaret Hospital, Hong Kong, Hong Kong|Queen Mary Hospital, Hong Kong, Hong Kong|Azienda Ospedaliero Universitaria di Parma, Parma, Iran, Islamic Republic of|ASST degli Spedali Civili di Brescia, Brescia, Italy|ASST di Cremona - Azienda Socio Sanitaria Territor, Cremona, Italy|ASST Fatebenefratelli Sacco, Milano, Italy|UOC Malattie Infettive e Tropicali, Azienda Ospedaliera di Padova, Padova PD, Italy|Malattie Infettive I, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy|Kyungpook National University Hospital, Daegu, Korea, Republic of|Seoul Medical Center, Seoul, Korea, Republic of|National Medical Center, Seoul, Korea, Republic of|National University Hospital, Singapore, Singapore|Singapore General Hospital, Singapore, Singapore|National Centre for Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore|Hospital Clinic de Barcelona, Barcelona, Spain|Hospital Universitario Cruces, Bizkaia, Spain|Hospital Universitario La Paz, Madrid, Spain|Hopitaux Universitaires de Genève, Genève 14, Switzerland|Ospedale Regionale di Locarno La Carità, Lugano, Switzerland|Universitätsspital Zürich, Zürich, Switzerland|Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan|China Medical University Hospital, Taichung, Taiwan|National Taiwan University Hospital, Taipei City, Taiwan | NCT04292730 | ||||
59 | https://ClinicalTrials.gov/show/NCT04315987 | Phase 1 | 5/1/2020 | 30 | Not yet recruiting | Biological: NestCell® | Interventional | 66 | NestCell® Mesenchymal Stem Cell to Treat Patients With Severe COVID-19 Pneumonia | HOPE | No Results Available | COVID-19 Pneumonia | Disappear time of ground-glass shadow in the lungs|Rate of mortality within 28-days|Change of Clinical symptoms including duration of fever and respiratory|Time of nucleic acid turning negative|CD4+ and CD8+ T cell count|Changes of blood oxygen|Side effects in the treatment group | Azidus Brasil|Cellavita Pesquisa Científica Ltda|Hospital Vera Cruz | 18 Years and older (Adult, Older Adult) | Industry|Other | Allocation: Non-Randomized|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/1/2020 | 3/20/2020 | 4/1/2020 | 3/31/2020 | Prevent Senior Private Operadora de Saúde LTDA., São Paulo, Brazil | NCT04315987 | |||
60 | https://ClinicalTrials.gov/show/NCT04273321 | Not Applicable | 5/1/2020 | 77 | Recruiting | Drug: Methylprednisolone | Interventional | 400 | Efficacy and Safety of Corticosteroids in COVID-19 | No Results Available | COVID-19|Novel Coronavirus Pneumonia | the incidence of treatment failure in 14 days|clinical cure incidence in 14 days|the duration of virus change to negative|mortality at day 30|ICU admission rate in 30 days | Beijing Chao Yang Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/30/2020 | 2/18/2020 | 2/14/2020 | 2/24/2020 | Hubei province hospital of integrated Chinese & Western Medicine, Wuhan, Hubei, China|Yichang first people's Hospital, Yichang, Hubei, China|Renmin Hospital of Wuhan University, Wuhan, China|Tianyou Hospital Affiliated to Wuhan University of science and technology, Wuhan, China|Union Hospital Affiliated to Tongji Medical College of Huazhong University of science and technology, Wuhan, China | NCT04273321 | ||||
61 | https://ClinicalTrials.gov/show/NCT04310228 | Not Applicable | 5/1/2020 | 54 | Recruiting | Drug: Favipiravir Combined With Tocilizumab|Drug: Favipiravir|Drug: Tocilizumab | Interventional | 150 | Favipiravir Combined With Tocilizumab in the Treatment of Corona Virus Disease 2019 | No Results Available | COVID-19 | Clinical cure rate|Viral nucleic acid test negative conversion rate and days from positive to negative|Duration of fever|Lung imaging improvement time|Mortality rate because of Corona Virus Disease 2019|Rate of non-invasive or invasive mechanical ventilation when respiratory failure occurs|Mean in-hospital time | Peking University First Hospital | 18 Years to 65 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/1/2020 | 3/17/2020 | 3/8/2020 | 3/17/2020 | Anhui Medical University Affiliated First Hospital, Hefei, Anhui, China|Guiqiang Wang, Beijing, Beijing, China|Peking University First Hospital, Beijing, Beijing, China|Cancer Hospital Union Hospital Tongji Medical College Huazhong University of Science and Technology, Wuhan, Hubei, China|Ezhou Central Hospital, Wuhan, Hubei, China|Huoshenshan Hospital of Wuhan, Wuhan, Hubei, China|Jinyintan Hospital of Wuhan, Wuhan, Hubei, China|Tongji Hospital of Huazhong University of Science and Technology, Wuhan, Hubei, China|West Hospital Union Hospital Huazhong University of Science and Technology, Wuhan, Hubei, China|Wuhan Pulmonary Hospital, Wuhan, Hubei, China|Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China | NCT04310228 | ||||
62 | https://ClinicalTrials.gov/show/NCT04261270 | Phase 3 | 5/1/2020 | 90 | Recruiting | Drug: ASC09F+Oseltamivir|Drug: Ritonavir+Oseltamivir|Drug: Oseltamivir | Interventional | 60 | A Randomized,Open,Controlled Clinical Study to Evaluate the Efficacy of ASC09F and Ritonavir for 2019-nCoV Pneumonia | No Results Available | 2019-nCoV Pneumonia | Rate of comprehensive adverse outcome|Time of clinical remission|Rate of no fever|Rate of no cough|Rate of no dyspnea|Rate of no need for oxygen inhalation|Rate of undetectable viral RNA|Rate of mechanical ventilation|Rate of ICU admission|Rate and time of CRP,ES,Biochemical criterion(CK,ALT,Mb)recovery | Tongji Hospital | 18 Years to 55 Years (Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 7/1/2020 | 2/7/2020 | 2/1/2020 | 3/17/2020 | Department and Institute of Infectious Disease, Wuhan, Hubei, China | NCT04261270 | ||||
63 | https://ClinicalTrials.gov/show/NCT04326452 | Not Applicable | 5/1/2020 | 32 | Not yet recruiting | Device: bidirectional oxygenation mouthpiece | Interventional | 5 | Treating COVID-19 With a Bidirectional Oxygenation Valve | No Results Available | Coronavirus Infection | Pulse oximetry level|Respiratory rate|Heart rate|Blood pressure|Systemic carbon dioxide | TMC HealthCare|PEEP Medical, LLC | 18 Years and older (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/1/2020 | 3/30/2020 | 3/30/2020 | 3/30/2020 | TMC HealthCare, Tucson, Arizona, United States|Emory Saint Joseph's Hospital, Atlanta, Georgia, United States | NCT04326452 | ||||
64 | https://ClinicalTrials.gov/show/NCT04320238 | Phase 3 | 5/1/2020 | 101 | Recruiting | Drug: recombinant human interferon Alpha-1b|Drug: thymosin alpha 1 | Interventional | 2944 | Experimental Trial of rhIFNα Nasal Drops to Prevent 2019-nCOV in Medical Staff | No Results Available | 2019 Novel Coronavirus Infection | new-onset COVID-19|Number of Participants with coronavirus related symptoms|Number of Participants with adverse effect | Shanghai Jiao Tong University School of Medicine | 18 Years to 65 Years (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Prevention | 6/1/2020 | 3/24/2020 | 1/21/2020 | 3/31/2020 | Taihe Hospital, Shiyan, Hubei, China | NCT04320238 | ||||
65 | https://ClinicalTrials.gov/show/NCT04274322 | 5/1/2020 | 90 | Not yet recruiting | Other: Nutrition support | Observational | 100 | Identifying Critically-ill Patients With COVID-19 Who Will Benefit Most From Nutrition Support Therapy: Validation of the NUTRIC Nutritional Risk Assessment Tool | No Results Available | Critically Ill|Coronavirus Infections | 28-day all cause mortality|All cause infection|The rate of complications|Length of ICU stay|Duration of mechanical ventilation | Peking University Third Hospital|School of Pharmaceutical Sciences, Peking University, Beijing, China|Department of Medicine, Queen's University, Kingston, Ontario, Canada | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Prospective | 7/1/2020 | 2/18/2020 | 2/1/2020 | 2/18/2020 | NCT04274322 | ||||||
66 | https://ClinicalTrials.gov/show/NCT04322279 | 5/1/2020 | 53 | Recruiting | Diagnostic Test: Serology|Genetic: Sequencing | Observational | 300 | Factors Associated With a Positive SARS-CoV-2 Serology in Contact Subjects at High/Moderate Risk of Coronavirus SARS-CoV-2 Infection (CoV-CONTACT-SERO) | No Results Available | Coronavirus | Number of Participants with positive serology in the 90 days following last contact|fever > 38°C, asthenia/fatigue/malaise, headache, thrills/sweating, myalgia/aches, cough, dyspnea, Acute Respiratory Distress Syndrome, diarrhea | Institut National de la Santé Et de la Recherche Médicale, France | Child, Adult, Older Adult | Other | Observational Model: Cohort|Time Perspective: Prospective | 5/1/2020 | 3/26/2020 | 3/9/2020 | 3/26/2020 | CIC 1425, Paris, France | NCT04322279 | |||||
67 | https://ClinicalTrials.gov/show/NCT04275388 | Not Applicable | 5/14/2020 | 90 | Not yet recruiting | Drug: Xiyanping injection|Drug: Lopinavir / ritonavir, alpha-interferon nebulization | Interventional | 348 | Xiyanping Injection for the Treatment of New Coronavirus Infected Pneumonia | No Results Available | 2019 Novel Coronavirus Pneumonia | Clinical recovery time|Complete fever time|Cough relief time|Virus negative time|Incidence of severe or critical neocoronavirus pneumonia | Jiangxi Qingfeng Pharmaceutical Co. Ltd. | 18 Years to 70 Years (Adult, Older Adult) | Industry | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 12/14/2021 | 2/19/2020 | 2/14/2020 | 2/19/2020 | NCT04275388 | |||||
68 | https://ClinicalTrials.gov/show/NCT04327674 | 5/15/2020 | 62 | Recruiting | Observational | 375 | The Use of Focused Lung Ultrasound in Patients Suspected of COVID-19 | No Results Available | COVID-19 | FLUS findings and respiratory failure|FLUS findings and chest x-ray.|FLUS findings and admission to intensive care.|FLUS findings and SAR-CoV-2 PCR-test result. | University of Aarhus | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Prospective | 5/15/2020 | 3/31/2020 | 3/14/2020 | 3/31/2020 | Lungemedicinsk Forskningsafdeling. Aarhus University Hospital, Aarhus, Denmark|Regionshospitalet Horsens., Horsens, Denmark | NCT04327674 | ||||||
69 | https://ClinicalTrials.gov/show/NCT04319211 | 5/15/2020 | 51 | Not yet recruiting | Other: Determination of physical activity, quality of life, stress levels of isolated people at home with the danger of coronavirus. | Observational | 200 | Effects of Social Isolation From Coronavirus; on Physical Activity, Quality of Life and Stress | COVID-19 | No Results Available | Healthy People | International Physical Activity Questionnaire (IPAQ)|Health-Related Quality of Life SF-12 Scale|Beck Depression Scale | Istanbul University-Cerrahpasa | 18 Years to 55 Years (Adult) | Other | Observational Model: Case-Only|Time Perspective: Cross-Sectional | 7/20/2020 | 3/24/2020 | 3/25/2020 | 3/24/2020 | Istanbul University Cerrahpasa, Istanbul, Turkey | NCT04319211 | ||||
70 | https://ClinicalTrials.gov/show/NCT04322188 | 5/19/2020 | 61 | Recruiting | Observational | 50 | An Observational Case-control Study of the Use of Siltuximab in ARDS Patients Diagnosed With COVID-19 Infection | SISCO | No Results Available | Severe Acute Respiratory Syndrome (ARDS) Secondary to SARS-COV-2 Infection | Cohort A: reduction of the need of invasive ventilation or 30-day mortality|Cohort B: reduction of mortality|Cohort A Reduction of the need of time of ventilatory support|Cohort B Percentage of patients that undergo to tracheostomy|Cohort B Improvement of the lung function assessed by radiologic findings | A.O. Ospedale Papa Giovanni XXIII | 18 Years and older (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Retrospective | 5/19/2020 | 3/26/2020 | 3/19/2020 | 3/31/2020 | ASST - Papa Giovanni XXIII, Bergamo, Italy | NCT04322188 | |||||
71 | https://ClinicalTrials.gov/show/NCT04320017 | 5/20/2020 | 61 | Recruiting | Diagnostic Test: Electrocardiogram and transthoracic echocardiography | Observational | 500 | Joint Use of Electrocardiogram and Transthoracic Echocardiography in an Observational Study to Monitor Cardio-vascular Events in Patients Diagnosed With COVID-19 | JOCOVID | No Results Available | COVID-19|Myocardial Injury|Myocarditis | Incidence of acute myocardial events in COVID-19 population at baseline and during hospital stay|Description of cardiovascular outcomes in the cohort|Prognosis role of baseline cardio-vascular caracteristics on patients survival|Prediction of cardio-vascular events with baseline characteristics|Characterization of inflammation on cardio-vascular outcomes | Groupe Hospitalier Pitie-Salpetriere | 16 Years and older (Child, Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Prospective | 5/20/2020 | 3/24/2020 | 3/20/2020 | 3/24/2020 | Clinical Investigation Center Pitié-Salpêtrière, Paris, France | NCT04320017 | ||||
72 | https://ClinicalTrials.gov/show/NCT04327349 | Not Applicable | 5/20/2020 | 53 | Enrolling by invitation | Biological: Convalescent Plasma | Interventional | 30 | Investigating Effect of Convalescent Plasma on COVID-19 Patients Outcome: A Clinical Trial | No Results Available | Coronavirus Infections | Mortality changes in day 10|Mortality changes in day 30|Changes of C-reactive protein|Changes of Interleukin 6|Changes of tumor necrosis factor-α|Changes of PaO2/FiO2 Ratio|Changes of CD3|Changes of CD4|Changes of CD8|Changes of CD4/CD8 ratio|Changes of lymphocyte count|Changes of leukocyte count|Changes of alanine transaminase (ALT)|Changes of aspartate transaminase (AST)|Changes of alkaline phosphatase (ALP)|Changes of lactate dehydrogenase (LDH)|Changes of creatine phosphokinase (CPK)|Changes of Creatine kinase-MB (CK-MB)|Changes of Specific IgG|Radiological findings|Number of days ventilated|Length of hospitalization | Mazandaran University of Medical Sciences | 30 Years to 70 Years (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 9/30/2020 | 3/31/2020 | 3/28/2020 | 3/31/2020 | Imam Khomeini Hospital, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran, Islamic Republic of | NCT04327349 | ||||
73 | https://ClinicalTrials.gov/show/NCT04323592 | Phase 2|Phase 3 | 5/20/2020 | 58 | Recruiting | Drug: Methylprednisolone|Other: standard care | Interventional | 104 | Efficacy of Methylprednisolone for Patients With COVID-19 Severe Acute Respiratory Syndrome | MP-C19 | No Results Available | Severe Acute Respiratory Syndrome (SARS) Pneumonia|Coronavirus Infections|ARDS, Human | Composite primary end-point|death|Admission to ICU|Endotracheal intubation (invasive mechanical ventilation)|reduction of C-reactive protein or CRP|Reduction of mechanical ventilation | University of Trieste | 18 Years to 80 Years (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/30/2020 | 3/26/2020 | 3/23/2020 | 3/27/2020 | Marco Confalonieri, Trieste, TS, Italy | "Study Protocol and Statistical Analysis Plan", https://ClinicalTrials.gov/ProvidedDocs/92/NCT04323592/Prot_SAP_000.pdf|"Informed Consent Form", https://ClinicalTrials.gov/ProvidedDocs/92/NCT04323592/ICF_001.pdf | NCT04323592 | ||
74 | https://ClinicalTrials.gov/show/NCT04328272 | Phase 3 | 5/28/2020 | 61 | Not yet recruiting | Drug: Hydroxychloroquine 200 Mg Oral Tablet | Interventional | 75 | Effectiveness of Hydroxychloroquine in Covid-19 Patients | Covid | No Results Available | COVID19 | National Early Warning Score equal to zero|C-reactive proteins|Lymphocyte Count|d-dimers | Prof. Dr. Umar Farooq|Ayub Medical College, Abbottabad | 18 Years to 50 Years (Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 6/28/2020 | 3/31/2020 | 3/28/2020 | 3/31/2020 | Ayub Teaching Institution, Abbottābād, K.p.k, Pakistan | NCT04328272 | |||
75 | https://ClinicalTrials.gov/show/NCT04273529 | Phase 2 | 5/30/2020 | 100 | Not yet recruiting | Drug: thalidomide|Drug: placebo | Interventional | 100 | The Efficacy and Safety of Thalidomide in the Adjuvant Treatment of Moderate New Coronavirus (COVID-19) Pneumonia | No Results Available | COVID-19 Thalidomide | Time to Clinical recoveryTime to Clinical Recovery (TTCR)|All cause mortality|Frequency of respiratory progression|Time to defervescence | First Affiliated Hospital of Wenzhou Medical University|Second Affiliated Hospital of Wenzhou Medical University|Wenzhou Central Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 6/30/2020 | 2/18/2020 | 2/20/2020 | 2/21/2020 | NCT04273529 | |||||
76 | https://ClinicalTrials.gov/show/NCT04298814 | 5/30/2020 | 84 | Not yet recruiting | Other: severe covid-19 pneumonia with ET | Observational | 120 | Safety Related Factors of Endotracheal Intubation in Patients With Severe Covid-19 Pneumonia | No Results Available | COVID-19|Endotracheal Intubation | Success rate of intubation|Infection rate of Anesthesiologist|Extubation time | Tongji Hospital | 18 Years to 90 Years (Adult, Older Adult) | Other | Observational Model: Case-Only|Time Perspective: Prospective | 7/30/2020 | 3/6/2020 | 3/7/2020 | 3/6/2020 | NCT04298814 | ||||||
77 | https://ClinicalTrials.gov/show/NCT04328480 | Phase 3 | 5/30/2020 | 90 | Not yet recruiting | Drug: Colchicine|Other: Local standard of care | Interventional | 2500 | The ECLA PHRI COLCOVID Trial | COLCOVID | No Results Available | COVID-19 | All-cause mortality|Composite outcome:composite of intubation for mechanical ventilation or death. | Estudios Clínicos Latino América|Population Health Research Institute | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 3/31/2020 | 3/1/2020 | 3/31/2020 | NCT04328480 | ||||
78 | https://ClinicalTrials.gov/show/NCT04306705 | 5/30/2020 | 100 | Recruiting | Drug: Tocilizumab|Other: Standard of care|Procedure: Continuous renal replacement therapy | Observational | 120 | Tocilizumab vs CRRT in Management of Cytokine Release Syndrome (CRS) in COVID-19 | TACOS | No Results Available | Covid-19|SARS|Cytokine Storm|Cytokine Release Syndrome|Tocilizumab | Proportion of Participants With Normalization of Fever and Oxygen Saturation Through Day 14|Duration of hospitalization|Proportion of Participants With Normalization of Fever Through Day 14|Change from baseline in white blood cell and differential count|Time to first negative in 2019 novel Corona virus RT-PCR test|All-cause mortality|Change from baseline in hsCRP|Change from baseline in cytokines IL-1β, IL-10, sIL-2R, IL-6, IL-8 and TNF-α|Change from baseline in proportion of CD4+CD3/CD8+CD3 T cells | Tongji Hospital|Hubei Xinhua Hospital|Wuhan No.1 Hospital|Wuhan central hospital | 18 Years to 80 Years (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 6/20/2020 | 3/13/2020 | 2/20/2020 | 3/17/2020 | Tongji Hospital, Wuhan, Hubei, China | NCT04306705 | ||||
79 | https://ClinicalTrials.gov/show/NCT04322565 | Phase 2 | 5/30/2020 | 59 | Not yet recruiting | Drug: Colchicine | Interventional | 100 | Colchicine Efficacy in COVID-19 Pneumonia | No Results Available | Coronavirus Infections|Pneumonia, Viral | Clinical improvement|Hospital discharge|Death|Clinical status|Mechanical venhtilation|Hospitalization|Time from death|Negativization COVID 19|Fever | Lucio Manenti|Azienda Ospedaliero-Universitaria di Parma | 18 Years to 85 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 3/26/2020 | 4/1/2020 | 3/26/2020 | NCT04322565 | |||||
80 | https://ClinicalTrials.gov/show/NCT04293887 | Early Phase 1 | 5/30/2020 | 90 | Not yet recruiting | Drug: Recombinant human interferon α1β | Interventional | 328 | Efficacy and Safety of IFN-α2β in the Treatment of Novel Coronavirus Patients | No Results Available | COVID-19|Recombinant Human Interferon α1β | The incidence of side effects|Time from patient enrollment to clinical remission|Proportion of patients with normal body|Proportion of patients without dyspnea|Proportion of patients without cough|Proportion|The negative conversion rate of new coronavirus nucleic acid|Frequency of serious adverse drug events. | Tongji Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 3/3/2020 | 3/1/2020 | 3/3/2020 | NCT04293887 | |||||
81 | https://ClinicalTrials.gov/show/NCT04321421 | Not Applicable | 5/31/2020 | 75 | Active, not recruiting | Other: hyperimmune plasma | Interventional | 49 | Hyperimmune Plasma for Critical Patients With COVID-19 | COV19-PLASMA | No Results Available | COVID-19 | death|time to extubation|length of intensive care unit stay|time to CPAP weaning|viral load|immune response | Foundation IRCCS San Matteo Hospital|OSPEDALE CARLO POMA ASST MANTOVA|OSPEDALE MAGGIORE LODI|OSPEDALE ASST CREMONA | 18 Years and older (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 5/31/2020 | 3/25/2020 | 3/17/2020 | 3/25/2020 | Catherine Klersy, Pavia, PV, Italy | NCT04321421 | |||
82 | https://ClinicalTrials.gov/show/NCT04324996 | Phase 1|Phase 2 | 5/31/2020 | 71 | Recruiting | Biological: NK cells,IL15-NK cells,NKG2D CAR-NK cells,ACE2 CAR-NK cells,NKG2D-ACE2 CAR-NK cells | Interventional | 90 | A Phase I/II Study of Universal Off-the-shelf NKG2D-ACE2 CAR-NK Cells for Therapy of COVID-19 | No Results Available | COVID-19 | Clinical response|Side effects in the treatment group | Chongqing Public Health Medical Center|Chongqing Sidemu Biotechnology Technology Co.,Ltd. | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|Primary Purpose: Treatment | 9/30/2020 | 3/27/2020 | 3/21/2020 | 3/27/2020 | Chongqing Public Health Medical Center, Chongqing, China | NCT04324996 | ||||
83 | https://ClinicalTrials.gov/show/NCT04325906 | Not Applicable | 5/31/2020 | 55 | Not yet recruiting | Device: high flow nasal cannula (HFNC)|Procedure: Prone positioning (PP) | Interventional | 162 | Early PP With HFNC Versus HFNC in COVID-19 Induced Moderate to Severe ARDS | No Results Available | Prone Positioning|High Flow Nasal Cannula|Acute Respiratory Distress Syndrome|Corona Virus Infection | Treatment failure|Intubation rate|Efficacy of PP | Rush University Medical Center|Medical College of Wisconsin | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 3/30/2020 | 4/6/2020 | 3/30/2020 | Rush University Medical Center, Chicago, Illinois, United States|Medical College of Wisconsin, Wauwatosa, Wisconsin, United States | NCT04325906 | ||||
84 | https://ClinicalTrials.gov/show/NCT04305574 | 5/31/2020 | 84 | Recruiting | Behavioral: Use of social media during COVID-19 | Observational | 5000 | Social Media Use During COVID-19 | No Results Available | Coronavirus|Depression|Anxiety|Stress | Assessment of COVID-19 situation|Depression, Anxiety and Stress Scale|Familiarity and trust in COVID-related rumours|Availability heuristic | Jean Liu|Yale-NUS College | 21 Years and older (Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Cross-Sectional | 5/31/2020 | 3/12/2020 | 3/8/2020 | 3/17/2020 | Yale-NUS College, Singapore, Singapore | NCT04305574 | |||||
85 | https://ClinicalTrials.gov/show/NCT04261907 | Not Applicable | 5/31/2020 | 114 | Not yet recruiting | Drug: ASC09/ritonavir group|Drug: lopinavir/ritonavir group | Interventional | 160 | Evaluating and Comparing the Safety and Efficiency of ASC09/Ritonavir and Lopinavir/Ritonavir for Novel Coronavirus Infection | No Results Available | 2019-nCoV | The incidence of composite adverse outcome|Time to recovery|Rate of no fever|Rate of no cough|Rate of no dyspnea|Rate of no requring supplemental oxygen|Rate of undectable viral RNA|Rate of mechanical ventilation|Rate of ICU admission|Time and rate of laboratory indicators related to disease improvement to return to normal | First Affiliated Hospital of Zhejiang University|Ascletis Pharmaceuticals Co., Ltd. | 18 Years to 75 Years (Adult, Older Adult) | Other|Industry | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 6/30/2020 | 2/10/2020 | 2/7/2020 | 2/10/2020 | NCT04261907 | |||||
86 | https://ClinicalTrials.gov/show/NCT04276987 | Phase 1 | 5/31/2020 | 106 | Not yet recruiting | Biological: MSCs-derived exosomes | Interventional | 30 | A Pilot Clinical Study on Inhalation of Mesenchymal Stem Cells Exosomes Treating Severe Novel Coronavirus Pneumonia | No Results Available | Coronavirus | Adverse reaction (AE) and severe adverse reaction (SAE)|Time to clinical improvement (TTIC)|Number of patients weaning from mechanical ventilation|Duration (days) of ICU monitoring|Duration (days) of vasoactive agents usage|Duration (days) of mechanical ventilation supply|Number of patients with improved organ failure|Rate of mortality | Ruijin Hospital|Shanghai Public Health Clinical Center|Wuhan Jinyintan Hospital, Wuhan, China|Cellular Biomedicine Group Ltd. | 18 Years to 75 Years (Adult, Older Adult) | Other|Industry | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 7/31/2020 | 2/19/2020 | 2/15/2020 | 2/25/2020 | NCT04276987 | |||||
87 | https://ClinicalTrials.gov/show/NCT04318431 | Not Applicable | 6/1/2020 | 61 | Not yet recruiting | Diagnostic Test: Data collection and rhinopharyngeal swab | Interventional | 600 | Prevalence of SARS -Cov2 Carriage in Asymptomatic and Mildly-symptomatic Children | COVILLE | No Results Available | Covid19 | Proportion of asymptomatic children or children with mild respiratory symptoms|Confirmed Cov2-SARS cases by age|Confirmed Cov2-SARS cases by symptoms|Viral load|Other respiratory viruses | Centre Hospitalier Intercommunal Creteil|ACTIV | 6 Months to 15 Years (Child) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Diagnostic | 6/1/2020 | 3/24/2020 | 4/1/2020 | 3/26/2020 | Cabinet du Dr Belaroussi, Boulogne, France|Cabinet du Dr Derkx, Champigny-sur-Marne, France|Cabinet du Dr Coicadan, Chennevières-sur-Marne, France|Cabinet du Dr Corrard, Combs-la-Ville, France|53 Boulevard De La Liberté, Les Lilas, France|157 Avenue du Général Leclerc, Maisons-Alfort, France|Cabinet du Dr Bodin, Montgeron, France|Cabinet du Dr Deberdt, Nogent-sur-Marne, France|Cabinet du Dr Wollner, Nogent-sur-Marne, France|Cabinet du Dr D'acremont, Paris, France|Cabinet du Dr Romain, Paris, France|Cabinet du Dr Turberg-Romain, Paris, France|Cabinet du Dr Michot, Paris, France|Cabinet du Dr Cohen, Saint-Maur-des-Fossés, France|Cabinet de Pédiatrie des Docteurs Ravilly et Bessa, Villejuif, France|13 Villa Beauséjour, Vincennes, France | NCT04318431 | |||
88 | https://ClinicalTrials.gov/show/NCT04311398 | 6/1/2020 | 79 | Not yet recruiting | Diagnostic Test: New QIAstat-Dx fully automatic multiple PCR detection platform | Observational | 100 | Development and Verification of a New Coronavirus Multiplex Nucleic Acid Detection System | No Results Available | COVID-19 | Sensitivity, spectivity turnaround time of the New QIAstat-Dx fully automatic multiple PCR detection platform | Huashan Hospital | 16 Years to 100 Years (Child, Adult, Older Adult) | Other | Observational Model: Cohort|Time Perspective: Retrospective | 12/1/2020 | 3/17/2020 | 3/14/2020 | 3/17/2020 | Huashan Hospital of Fudan University, Shanghai, Shanghai, China | NCT04311398 | |||||
89 | https://ClinicalTrials.gov/show/NCT04255017 | Phase 4 | 6/1/2020 | 121 | Recruiting | Drug: Abidol hydrochloride|Drug: Oseltamivir|Drug: Lopinavir/ritonavir | Interventional | 400 | A Prospective/Retrospective,Randomized Controlled Clinical Study of Antiviral Therapy in the 2019-nCoV Pneumonia | No Results Available | 2019-nCoV | Rate of disease remission|Time for lung recovery|Rate of no fever|Rate of respiratory symptom remission|Rate of lung imaging recovery|Rate of CRP,ES,Biochemical criterion(CK,ALT,Mb) recovery|Rate of undetectable viral RNA | Tongji Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 7/1/2020 | 2/5/2020 | 2/1/2020 | 3/17/2020 | Department and Institute of Infectious Disease, Wuhan, Hubei, China | NCT04255017 | ||||
90 | https://ClinicalTrials.gov/show/NCT04254874 | Phase 4 | 6/1/2020 | 121 | Recruiting | Drug: Abidol hydrochloride|Drug: Abidol Hydrochloride combined with Interferon atomization | Interventional | 100 | A Prospective/Retrospective,Randomized Controlled Clinical Study of Interferon Atomization in the 2019-nCoV Pneumonia | No Results Available | 2019-nCoV | Rate of disease remission|Time for lung recovery|Rate of no fever|Rate of respiratory symptom remission|Rate of lung imaging recovery|Rate of CRP,ES,Biochemical criterion (CK,ALT,Mb)recovery|Rate of undetectable viral RNA | Tongji Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 7/1/2020 | 2/5/2020 | 2/1/2020 | 3/17/2020 | Department and Institute of Infectious Disease, Wuhan, Hubei, China | NCT04254874 | ||||
91 | https://ClinicalTrials.gov/show/NCT04263402 | Phase 4 | 6/1/2020 | 121 | Recruiting | Drug: Methylprednisolone | Interventional | 100 | The Efficacy of Different Hormone Doses in 2019-nCoV Severe Pneumonia | No Results Available | 2019-nCoV Severe Pneumonia | Rate of disease remission|Rate and time of entering the critical stage|Rate of normal tempreture|Rate of respiratory symptom remission|Rate of lung imaging recovery|Rate of laboratory indicator recovery|Rate of undetectable viral RNA | Tongji Hospital | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Single (Participant)|Primary Purpose: Treatment | 7/1/2020 | 2/10/2020 | 2/1/2020 | 3/17/2020 | Department and Institute of Infectious Disease, Wuhan, Hubei, China | NCT04263402 | ||||
92 | https://ClinicalTrials.gov/show/NCT04324684 | 6/3/2020 | 61 | Not yet recruiting | Observational | 198 | Prognostic Factors Keeping Track for Covid19 Pneumonia | NIKE_C19 | No Results Available | Pneumonia, Viral|Hypertension|Diabetes Mellitus|Obesity|Cardiovascular Diseases|Obstructive Lung Disease | mean recovery rate|comparison of time to improvement|organ failure|efficacy of treatments | Catholic University of the Sacred Heart | 18 Years to 100 Years (Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Prospective | 6/30/2020 | 3/27/2020 | 4/3/2020 | 3/27/2020 | NCT04324684 | ||||||
93 | https://ClinicalTrials.gov/show/NCT04304053 | Phase 3 | 6/15/2020 | 89 | Recruiting | Drug: Antiviral treatment and prophylaxis|Other: Standard Public Health measures | Interventional | 3040 | Treatment of COVID-19 Cases and Chemoprophylaxis of Contacts as Prevention | HCQ4COV19 | No Results Available | COVID-19 | Effectiveness of chemoprophylaxis assessed by incidence of secondary COVID-19 cases|The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at days 3|The mortality rate of subjects at weeks 2|Proportion of participants that drop out of study|Proportion of participants that show non-compliance with study drug | Fundacio Lluita Contra la SIDA|Germans Trias i Pujol Hospital|Department of Health, Generalitat de Catalunya|FUNDACIÓN FLS DE LUCHA CONTRA EL SIDA, LAS ENFERMEDADES INFECCIOSAS Y LA PROMOCIÓN DE LA SALUD Y LA CIENCIA|Laboratorios Gebro Pharma SA|Laboratorios Rubió|Institut Catala de Salut | 18 Years and older (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Prevention | 6/15/2020 | 3/11/2020 | 3/18/2020 | 3/24/2020 | CAP II Sant Fèlix, Sabadell, Barcelona, Spain|Gerència Territorial Catalunya Central, Sant Fruitós De Bages, Barcelona, Spain|Centre de Salut Isabel Roig-Casernes de Sant Andreu, Barcelona, Spain | NCT04304053 | |||
94 | https://ClinicalTrials.gov/show/NCT04285190 | Not Applicable | 6/15/2020 | 110 | Not yet recruiting | Drug: T89 | Interventional | 120 | The Effect of T89 on Improving Oxygen Saturation and Clinical Symptoms in Patients With COVID-19 | No Results Available | Coronavirus Disease 2019|Novel Coronavirus Pneumonia | The time to oxygen saturation recovery to normal level (≥97%)|The proportion of patients with normal level of oxygen saturation(≥97%)|The degree of remission of symptoms of patients, including: fatigue, nausea, vomiting, chest tightness, shortness of breath, etc.|The time to the myocardial enzyme spectrum recovery to normal after treatment|The proportion of the patients with normal myocardial enzyme spectrum after treatment|The time to the electrocardiogram recovery to normal level after treatment|The proportion of the patients with normal electrocardiogram after treatment|The time to the hemodynamics recovery to normal after treatment|The proportion of the patients with normal hemodynamics after treatment|The time to exacerbation or remission of the disease after treatment;|The proportion of the patients with exacerbation or remission of disease after treatment|The proportion of patients who need other treatment (e.g. heparin, anticoagulants) due to microcirculation disorders|The all-cause mortality rate|The proportion of patients with acidosis|The total duration of the patients in-hospital|The total duration of oxygen inhalation during treatment|The oxygen flow rate during treatment|The oxygen concentration during treatment | Tasly Pharmaceuticals, Inc. | 18 Years to 85 Years (Adult, Older Adult) | Industry | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 9/15/2020 | 2/26/2020 | 2/26/2020 | 2/26/2020 | NCT04285190 | |||||
95 | https://ClinicalTrials.gov/show/NCT04305106 | Not Applicable | 6/30/2020 | 105 | Recruiting | Drug: Bevacizumab | Interventional | 140 | Bevacizumab in Severe or Critically Severe Patients With COVID-19 Pneumonia-RCT | BEST-RCT | No Results Available | COVID-19 Pneumonia | The time from randomization to clinical improvement | Qilu Hospital of Shandong University|Renmin Hospital of Wuhan University|Ialy Moriggia Pelascini Gravedona Hospital S.p.A|Wuhan University|Jiangbei Union Hospital of Huazhong University of science and technology|Shandong Provincial Chest Hospital | 18 Years to 80 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Triple (Participant, Care Provider, Outcomes Assessor)|Primary Purpose: Treatment | 7/31/2020 | 3/12/2020 | 3/17/2020 | 3/26/2020 | Qilu Hospital of Shandong University, Jinan, Shandong, China | NCT04305106 | |||
96 | https://ClinicalTrials.gov/show/NCT04313322 | Phase 1 | 6/30/2020 | 106 | Recruiting | Biological: WJ-MSCs | Interventional | 5 | Treatment of COVID-19 Patients Using Wharton's Jelly-Mesenchymal Stem Cells | No Results Available | Use of Stem Cells for COVID-19 Treatment | Clinical outcome|CT Scan|RT-PCR results | Stem Cells Arabia | 18 Years and older (Adult, Older Adult) | Other | Intervention Model: Single Group Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 9/30/2020 | 3/18/2020 | 3/16/2020 | 3/18/2020 | Stem Cells Arabia, Amman, Jordan | NCT04313322 | ||||
97 | https://ClinicalTrials.gov/show/NCT04273646 | Not Applicable | 6/30/2020 | 135 | Not yet recruiting | Biological: UC-MSCs|Drug: Placebo | Interventional | 48 | Study of Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Novel Coronavirus Severe Pneumonia | No Results Available | 2019 Novel Coronavirus Pneumonia|COVID-19 | Pneumonia severity index|Oxygenation index (PaO2/FiO2)|Side effects in the UC-MSCs treatment group|28-days survival|Sequential organ failure assessment|C-reactive protein|Procalcitonin|Lymphocyte count|CD3+, CD4+ and CD8+ T celll count|CD4+/CD8+ratio | Wuhan Union Hospital, China|Wuhan Hamilton Bio-technology Co., Ltd, China. | 18 Years to 65 Years (Adult, Older Adult) | Other | Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 2/15/2022 | 2/18/2020 | 2/16/2020 | 2/21/2020 | Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China | NCT04273646 | ||||
98 | https://ClinicalTrials.gov/show/NCT04322344 | Phase 2|Phase 3 | 6/30/2020 | 99 | Recruiting | Drug: Escin|Drug: standard therapy | Interventional | 120 | Escin in Patients With Covid-19 Infection | add-on-COV2 | No Results Available | Coronavirus Infections | Mortality rate|Clinical status evaluated in agreement with guidelines|The differences in oxygen intake methods|Time of hospitalization (days)|Time of hospitalization in intensive care units|Pulmonary function | University of Catanzaro|Azienda Ospedaliera Pugliese Ciaccio|Azienda Ospedaliera Policlinico "Mater Domini" | 18 Years to 75 Years (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: Double (Participant, Care Provider)|Primary Purpose: Supportive Care | 8/30/2020 | 3/26/2020 | 3/23/2020 | 3/27/2020 | Luca Gallelli, Catanzaro, Italy | NCT04322344 | |||
99 | https://ClinicalTrials.gov/show/NCT04322513 | 6/30/2020 | 98 | Recruiting | Diagnostic Test: Biomarkers expression | Observational | 110 | Biomarkers for Identification of SARS-COV-2 Infection | B-DT-COV2 | No Results Available | Coronavirus | Biomarkers expression|Liver Biomarkers expression|biomarkers expression (microRNAs, oxidative stress, IL-2, IL-6, TNF-alfa, leukocytes, subtypes lymphocytes) after treatment | University of Catanzaro|Azienda Ospedaliera Pugliese Ciaccio|Azienda Ospedaliera Policlinico "Mater Domini" | 14 Years to 75 Years (Child, Adult, Older Adult) | Other | Observational Model: Case-Control|Time Perspective: Prospective | 8/30/2020 | 3/26/2020 | 3/24/2020 | 3/27/2020 | Luca Gallelli, Catanzaro, Italy | NCT04322513 | ||||
100 | https://ClinicalTrials.gov/show/NCT04280588 | Phase 2 | 7/1/2020 | 130 | Recruiting | Drug: Fingolimod 0.5 mg | Interventional | 30 | Fingolimod in COVID-19 | No Results Available | Coronavirus Disease (COVID-19) | The change of pneumonia severity on X-ray images | First Affiliated Hospital of Fujian Medical University | 18 Years to 80 Years (Adult, Older Adult) | Other | Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Masking: None (Open Label)|Primary Purpose: Treatment | 7/1/2020 | 2/21/2020 | 2/22/2020 | 2/21/2020 | Wan-Jin Chen, Fuzhou, China | NCT04280588 |