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Source, April 18:
https://clinicaltrials.gov/ct2/results?cond=COVID-19
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URLPhases
Primary Completion Date
Length (days)StatusInterventionsStudy TypeEnrollmentTitleAcronymStudy ResultsConditions
Outcome Measures
Sponsor/Collaborators
AgeFunded BysStudy DesignsCompletion DateFirst PostedStart Date
Last Update Posted
Locations
Study Documents
NCT Number
3
https://ClinicalTrials.gov/show/NCT04280705Phase 34/1/20231,135
https://docs.google.com/spreadsheets/d/15r-EqvDTJJLMhOaEzPjrEcFAMPPPk9-FTgdt-qWG6lY/edit#gid=2022203840&range=2:2
Drug: RemdesivirInterventional440Adaptive 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
4/1/20232/21/20202/21/20203/27/2020
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/NCT043227865/31/20166,725
Active, not recruiting
Drug: ACE inhibitorObservational1302508
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
3/31/20203/26/20201/1/19983/26/2020NCT04322786
5
https://ClinicalTrials.gov/show/NCT043026882/10/202062CompletedObservational669
Accurate Classification System for Patients With COVID-19 Pneumonitis
No Results Available
Pneumonitissurvival status
Renmin Hospital of Wuhan University
Child, Adult, Older Adult
Other
Observational Model: Other|Time Perspective: Retrospective
3/4/20203/10/202012/10/20193/10/2020
Renmin Hospital of Wuhan University, Wuhan, Hubei, China
NCT04302688
6
https://ClinicalTrials.gov/show/NCT042840462/18/202018CompletedOther: CT scoreObservational39CT 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
2/18/20202/25/20201/31/20202/25/2020
Wuhan third hospital, Wuhan, Hubei, China
NCT04284046
7
https://ClinicalTrials.gov/show/NCT042858012/25/202011CompletedObservational8
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
2/25/20202/26/20202/14/20203/10/2020
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/NCT04293692Not Applicable2/25/20201WithdrawnBiological: UC-MSCs|Other: PlaceboInterventional0
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
2/25/20203/3/20202/24/20203/18/2020
Puren Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, Hubei, China
NCT04293692
9
https://ClinicalTrials.gov/show/NCT04261517Phase 32/25/202019CompletedDrug: HydroxychloroquineInterventional30
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
2/25/20202/7/20202/6/20203/24/2020
Shanghai Public Health Clinical Center, Shanghai, Shanghai, China|Shanghai Public Health Clinical Center, Shanghai, Shanghai, China
NCT04261517
10
https://ClinicalTrials.gov/show/NCT043162992/28/20202CompletedObservational287Acute 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
3/8/20203/20/20202/26/20203/30/2020
Hankou Hospital, Wuhan, Hubei, China
NCT04316299
11
https://ClinicalTrials.gov/show/NCT04323332Phase 33/1/20200Not yet recruitingDrug: Traditional Chinese Medicine PrescriptionInterventional50Traditional 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
4/1/20203/26/20203/1/20203/26/2020
Hao Li, Beijing, Beijing, China
NCT04323332
12
https://ClinicalTrials.gov/show/NCT04304313Phase 33/1/202021RecruitingDrug: Sildenafil citrate tabletsInterventional10A 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
11/9/20203/11/20202/9/20203/17/2020
Department and Institute of Infectious Disease, Wuhan, Hubei, China
NCT04304313
13
https://ClinicalTrials.gov/show/NCT04281693Not Applicable3/1/202029Not yet recruiting
Diagnostic Test: Standard screening strategy|Diagnostic Test: New screening strategy
Interventional230
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
3/1/20202/24/20202/1/20202/24/2020
the Fifth Medical Center of Chinese PLA General Hospital, Beijing, Beijing, China
NCT04281693
14
https://ClinicalTrials.gov/show/NCT042929643/13/202012CompletedObservational201Prognostic 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
3/13/20203/3/20203/1/20203/17/2020
The First Affiliated Hospital of Chongqing Medical University, Chongqing, China
NCT04292964
15
https://ClinicalTrials.gov/show/NCT043124643/15/202074
Enrolling by invitation
Other: nonObservational500Myocardial 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
3/18/20203/18/20201/1/20203/18/2020
Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China
NCT04312464
16
https://ClinicalTrials.gov/show/NCT043193153/16/20205RecruitingOther: surveyObservational400
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
3/16/20203/24/20203/11/20203/24/2020
Assiut University Hospitals, Assiut, Egypt
NCT04319315
17
https://ClinicalTrials.gov/show/NCT04320953Not Applicable3/16/20200CompletedDevice: Non-contact MCE systemInterventional1Non-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
3/16/20203/25/20203/16/20203/25/2020
Changhai Hospital, Shanghai, China
NCT04320953
18
https://ClinicalTrials.gov/show/NCT04306055Not Applicable3/19/20207Not yet recruiting
Other: Questionnaire with precaution information|Other: Experimental: Questionnaire without precaution information
Interventional1500Blood 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
4/9/20203/12/20203/12/20203/12/2020NCT04306055
19
https://ClinicalTrials.gov/show/NCT04291729Phase 43/19/202031CompletedDrug: Ganovo+ritonavir+/-Interferon nebulizationInterventional11
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
3/19/20203/2/20202/17/20203/24/2020
The Ninth Hospital of Nanchang, Nanchang, Jiangxi, China
NCT04291729
20
https://ClinicalTrials.gov/show/NCT043213693/23/202014Completed
Diagnostic Test: Testing Sensitivity for SARS-CoV-2 Virus in Symptomatic Individuals
Observational533
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
3/23/20203/25/20203/9/20203/25/2020
Everett Clinic, Seattle, Washington, United States
NCT04321369
21
https://ClinicalTrials.gov/show/NCT043183013/28/20207
Active, not recruiting
Observational275Hypertension in Patients Hospitalized With COVID-19HT-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
3/30/20203/23/20203/21/20203/24/2020
Hankou Hospital, Hankou, Hubei, China
NCT04318301
22
https://ClinicalTrials.gov/show/NCT042727103/31/202066WithdrawnObservational0
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
4/30/20202/17/20201/25/20203/17/2020
The First Affiliated Hospital of Chongqing Medical University, Chongqing, China
NCT04272710
23
https://ClinicalTrials.gov/show/NCT042809133/31/202038WithdrawnOther: retrospective analysisObservational0Clinical 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
3/31/20202/21/20202/22/20203/19/2020
HuiZhou Municipal Central Hospital, Huizhou, Guangdong, China
NCT04280913
24
https://ClinicalTrials.gov/show/NCT04287686Not Applicable4/1/202060Withdrawn
Drug: Recombinant human angiotensin-converting enzyme 2 (rhACE2)
Interventional0
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
4/1/20202/27/20202/1/20203/17/2020
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
4/1/202060RecruitingDrug: Bevacizumab InjectionInterventional20
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
5/1/20202/19/20202/1/20202/19/2020
Qilu Hospital of Shandong University, Jinan, Shandong, China
NCT04275414
26
https://ClinicalTrials.gov/show/NCT04315480Phase 24/1/202031Not yet recruitingDrug: TocilizumabInterventional30Tocilizumab 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
5/1/20203/19/20203/1/20203/19/2020
Università Politecnica delle Marche, Ancona, AN, Italy
"Study Protocol", https://ClinicalTrials.gov/ProvidedDocs/80/NCT04315480/Prot_000.pdf
NCT04315480
27
https://ClinicalTrials.gov/show/NCT043284544/2/202063RecruitingOther: retrospective analysisObservational120
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
4/15/20203/31/20201/30/20203/31/2020
Shanghai 10th People's Hospital, Shanghai, Shanghai, China
NCT04328454
28
https://ClinicalTrials.gov/show/NCT04257656Phase 34/3/202057RecruitingDrug: Remdesivir|Drug: Remdesivir placeboInterventional453Severe 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
5/1/20202/6/20202/6/20202/24/2020
Bin Cao, Beijing, Beijing, China
NCT04257656
29
https://ClinicalTrials.gov/show/NCT043278044/3/20209RecruitingDiagnostic Test: Odd/Even birth year intervention groupsObservational120
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
4/10/20203/31/20203/25/20203/31/2020
Everett Clinic, Seattle, Washington, United States
NCT04327804
30
https://ClinicalTrials.gov/show/NCT043184184/10/202018Not yet recruitingObservational5000
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
4/30/20203/24/20203/23/20203/24/2020
IRCCS Neuromed, Department of Epidemiology and Prevention, Pozzilli, Italy
NCT04318418
31
https://ClinicalTrials.gov/show/NCT04252664Phase 34/10/202058RecruitingDrug: Remdesivir|Drug: Remdesivir placeboInterventional308Mild/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
4/27/20202/5/20202/12/20202/24/2020
Jin Yin-tan hospital, Wu Han, Hubei, China
NCT04252664
32
https://ClinicalTrials.gov/show/NCT043247364/10/202011Not yet recruitingOther: no interventional studyObservational300"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
5/8/20203/27/20203/30/20203/31/2020NCT04324736
33
https://ClinicalTrials.gov/show/NCT04273763Not Applicable4/15/202059
Enrolling by invitation
Drug: Bromhexine Hydrochloride Tablets|Drug: Arbidol Hydrochloride Granules|Drug: Recombinant Human Interferon α2b Spray
Interventional60
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
4/30/20202/18/20202/16/20203/23/2020
The Second AffIliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China
NCT04273763
34
https://ClinicalTrials.gov/show/NCT042603084/15/202072RecruitingObservational30000
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
4/20/20202/7/20202/3/20202/7/2020
Tongji Hospital,Tongji Medical College Affiliated,Huazhong University of Science & Technology, Wuhan, Hubei, China
NCT04260308
35
https://ClinicalTrials.gov/show/NCT043074594/19/202031Not yet recruitingOther: standard operating proceduresObservational50
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
12/31/20203/13/20203/19/20203/17/2020
Luigi Sacco University Hospital, Milan, Lombardia, Italy
NCT04307459
36
https://ClinicalTrials.gov/show/NCT043158704/20/2020110Recruiting
Other: pregnant women with laboratory-confirmed 2019-n-CoV
Observational20
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
4/30/20203/20/20201/1/20203/20/2020
University of Naples Federico II, Napoli, Italy
NCT04315870
37
https://ClinicalTrials.gov/show/NCT04308668Phase 34/21/202035RecruitingDrug: Hydroxychloroquine|Other: PlaceboInterventional3000
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
5/12/20203/16/20203/17/20203/27/2020
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/NCT04324489Not Applicable4/25/202050RecruitingDrug: DAS181Interventional4DAS181 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
4/30/20203/27/20203/6/20203/27/2020
Renmin Hospital of Wuhan University, Wuhan, Hubei, China
NCT04324489
39
https://ClinicalTrials.gov/show/NCT04323345Phase 34/25/202031Not yet recruitingDietary Supplement: Natural Honey|Other: Standard CareInterventional1000
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
5/10/20203/26/20203/25/20203/26/2020
Mahmoud Tantawy, Cairo, Egypt
NCT04323345
40
https://ClinicalTrials.gov/show/NCT04244591
Phase 2|Phase 3
4/25/202090RecruitingDrug: methylprednisolone therapy|Other: Standard careInterventional80
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
12/25/20201/28/20201/26/20202/13/2020
Medical ICU,Peking Union Medical College Hospital, Beijing, Beijing, China
NCT04244591
41
https://ClinicalTrials.gov/show/NCT043275314/26/202031
Active, not recruiting
Behavioral: turkish physiciansObservational200
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
4/28/20203/31/20203/26/20203/31/2020
Pinar Yalcin Bahat, Istanbul, İ̇stanbul, Turkey
NCT04327531
42
https://ClinicalTrials.gov/show/NCT042759474/30/202076RecruitingOther: nCapp, a cell phone-based auto-diagnosis systemObservational450The 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
5/31/20202/19/20202/14/20202/19/2020
Renmin Hospital of Wuhan University, Wuhan, Hubei, China
NCT04275947
43
https://ClinicalTrials.gov/show/NCT04273581Phase 24/30/202072Not yet recruitingDrug: placebo|Drug: ThalidomideInterventional40
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
5/30/20202/18/20202/18/20202/21/2020NCT04273581
44
https://ClinicalTrials.gov/show/NCT04251767Not Applicable4/30/202085WithdrawnOther: washed microbiota transplantation|Other: placeboInterventional0
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
4/30/20202/5/20202/5/20203/17/2020
Medical Center for Digestive Diseases, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
NCT04251767
45
https://ClinicalTrials.gov/show/NCT04268537Phase 24/30/202080Not yet recruiting
Drug: PD-1 blocking antibody+standard treatment|Drug: Thymosin+standard treatment|Other: standard treatment
Interventional120Immunoregulatory 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
10/31/20202/13/20202/10/20202/13/2020NCT04268537
46
https://ClinicalTrials.gov/show/NCT04261426
Phase 2|Phase 3
4/30/202080Not yet recruitingDrug: Intravenous Immunoglobulin|Other: Standard careInterventional80
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
6/30/20202/7/20202/10/20202/7/2020NCT04261426
47
https://ClinicalTrials.gov/show/NCT043169494/30/202041RecruitingObservational350Predictors 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
5/31/20203/20/20203/20/20203/27/2020
University of Bologna - Department of Medical and Surgical Sciences, Bologna, Italy
NCT04316949
48
https://ClinicalTrials.gov/show/NCT04320277Phase 34/30/202045RecruitingDrug: BaricitinibInterventional60
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
4/30/20203/24/20203/16/20203/24/2020
Fabrizio Cantini, Prato, Tuscany, Italy
NCT04320277
49
https://ClinicalTrials.gov/show/NCT04264858Not Applicable4/30/202044Not yet recruitingDrug: Immunoglobulin of cured patients|Drug: γ-GlobulinInterventional10
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
5/31/20202/11/20203/17/20203/17/2020
Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China
NCT04264858
50
https://ClinicalTrials.gov/show/NCT043190164/30/2020120Recruiting
Other: pregnant women with laboratory-confirmed 2019-n-CoV
Observational20
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
5/1/20203/24/20201/1/20203/24/2020
Gabriele Saccone, Napoli, Italy
NCT04319016
51
https://ClinicalTrials.gov/show/NCT042923274/30/2020120
Active, not recruiting
Observational400
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
7/31/20203/3/20201/1/20203/3/2020
Fujian Provincial Hospital, Fuzhou, Fujian, China
NCT04292327
52
https://ClinicalTrials.gov/show/NCT04269525Phase 24/30/202084RecruitingBiological: UC-MSCsInterventional10
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
9/30/20202/13/20202/6/20202/17/2020
Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China
NCT04269525
53
https://ClinicalTrials.gov/show/NCT040613824/30/2020198RecruitingProcedure: venepunctureObservational2300Sero-epidemiological Survey of England in 2019/2020STORY
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
11/30/20208/19/201910/15/20193/24/2020
Centre for Clinical Vaccinology & Tropical Medicine (CCVTM), Oxford, Oxfordshire, United Kingdom
NCT04061382
54
https://ClinicalTrials.gov/show/NCT042559404/30/2020101RecruitingObservational120002019-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
4/30/20202/5/20201/20/20202/5/2020
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/NCT043064975/1/202060RecruitingDrug: TCM prescriptionsObservational340
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
5/1/20203/13/20203/2/20203/17/2020
Huai'an fourth people's Hospital, Huaian, Jiangsu, China
NCT04306497
56
https://ClinicalTrials.gov/show/NCT04307693Phase 25/1/202051RecruitingDrug: Lopinavir/ritonavir|Drug: Hydroxychloroquine sulfateInterventional150
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
5/1/20203/13/20203/11/20203/13/2020
Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea, Republic of
NCT04307693
57
https://ClinicalTrials.gov/show/NCT04292899Phase 35/1/202056RecruitingDrug: Remdesivir|Drug: Standard of CareInterventional400
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
5/1/20203/3/20203/6/20203/31/2020
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/NCT04292730Phase 35/1/202047RecruitingDrug: Remdesivir|Drug: Standard of CareInterventional600
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
5/1/20203/3/20203/15/20203/31/2020
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/NCT04315987Phase 15/1/202030Not yet recruitingBiological: NestCell®Interventional66
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
6/1/20203/20/20204/1/20203/31/2020
Prevent Senior Private Operadora de Saúde LTDA., São Paulo, Brazil
NCT04315987
60
https://ClinicalTrials.gov/show/NCT04273321Not Applicable5/1/202077RecruitingDrug: MethylprednisoloneInterventional400Efficacy 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
5/30/20202/18/20202/14/20202/24/2020
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/NCT04310228Not Applicable5/1/202054Recruiting
Drug: Favipiravir Combined With Tocilizumab|Drug: Favipiravir|Drug: Tocilizumab
Interventional150
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
5/1/20203/17/20203/8/20203/17/2020
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/NCT04261270Phase 35/1/202090Recruiting
Drug: ASC09F+Oseltamivir|Drug: Ritonavir+Oseltamivir|Drug: Oseltamivir
Interventional60
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
7/1/20202/7/20202/1/20203/17/2020
Department and Institute of Infectious Disease, Wuhan, Hubei, China
NCT04261270
63
https://ClinicalTrials.gov/show/NCT04326452Not Applicable5/1/202032Not yet recruitingDevice: bidirectional oxygenation mouthpieceInterventional5Treating 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
6/1/20203/30/20203/30/20203/30/2020
TMC HealthCare, Tucson, Arizona, United States|Emory Saint Joseph's Hospital, Atlanta, Georgia, United States
NCT04326452
64
https://ClinicalTrials.gov/show/NCT04320238Phase 35/1/2020101Recruiting
Drug: recombinant human interferon Alpha-1b|Drug: thymosin alpha 1
Interventional2944
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
6/1/20203/24/20201/21/20203/31/2020
Taihe Hospital, Shiyan, Hubei, China
NCT04320238
65
https://ClinicalTrials.gov/show/NCT042743225/1/202090Not yet recruitingOther: Nutrition supportObservational100
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
7/1/20202/18/20202/1/20202/18/2020NCT04274322
66
https://ClinicalTrials.gov/show/NCT043222795/1/202053RecruitingDiagnostic Test: Serology|Genetic: SequencingObservational300
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
5/1/20203/26/20203/9/20203/26/2020
CIC 1425, Paris, France
NCT04322279
67
https://ClinicalTrials.gov/show/NCT04275388Not Applicable5/14/202090Not yet recruiting
Drug: Xiyanping injection|Drug: Lopinavir / ritonavir, alpha-interferon nebulization
Interventional348
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
12/14/20212/19/20202/14/20202/19/2020NCT04275388
68
https://ClinicalTrials.gov/show/NCT043276745/15/202062RecruitingObservational375
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
5/15/20203/31/20203/14/20203/31/2020
Lungemedicinsk Forskningsafdeling. Aarhus University Hospital, Aarhus, Denmark|Regionshospitalet Horsens., Horsens, Denmark
NCT04327674
69
https://ClinicalTrials.gov/show/NCT043192115/15/202051Not yet recruiting
Other: Determination of physical activity, quality of life, stress levels of isolated people at home with the danger of coronavirus.
Observational200
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
7/20/20203/24/20203/25/20203/24/2020
Istanbul University Cerrahpasa, Istanbul, Turkey
NCT04319211
70
https://ClinicalTrials.gov/show/NCT043221885/19/202061RecruitingObservational50
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
5/19/20203/26/20203/19/20203/31/2020
ASST - Papa Giovanni XXIII, Bergamo, Italy
NCT04322188
71
https://ClinicalTrials.gov/show/NCT043200175/20/202061Recruiting
Diagnostic Test: Electrocardiogram and transthoracic echocardiography
Observational500
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
5/20/20203/24/20203/20/20203/24/2020
Clinical Investigation Center Pitié-Salpêtrière, Paris, France
NCT04320017
72
https://ClinicalTrials.gov/show/NCT04327349Not Applicable5/20/202053
Enrolling by invitation
Biological: Convalescent PlasmaInterventional30
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
9/30/20203/31/20203/28/20203/31/2020
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
5/20/202058RecruitingDrug: Methylprednisolone|Other: standard careInterventional104
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
5/30/20203/26/20203/23/20203/27/2020
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/NCT04328272Phase 35/28/202061Not yet recruitingDrug: Hydroxychloroquine 200 Mg Oral TabletInterventional75Effectiveness of Hydroxychloroquine in Covid-19 PatientsCovid
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
6/28/20203/31/20203/28/20203/31/2020
Ayub Teaching Institution, Abbottābād, K.p.k, Pakistan
NCT04328272
75
https://ClinicalTrials.gov/show/NCT04273529Phase 25/30/2020100Not yet recruitingDrug: thalidomide|Drug: placeboInterventional100
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
6/30/20202/18/20202/20/20202/21/2020NCT04273529
76
https://ClinicalTrials.gov/show/NCT042988145/30/202084Not yet recruitingOther: severe covid-19 pneumonia with ETObservational120
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
7/30/20203/6/20203/7/20203/6/2020NCT04298814
77
https://ClinicalTrials.gov/show/NCT04328480Phase 35/30/202090Not yet recruitingDrug: Colchicine|Other: Local standard of careInterventional2500The ECLA PHRI COLCOVID TrialCOLCOVID
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
6/30/20203/31/20203/1/20203/31/2020NCT04328480
78
https://ClinicalTrials.gov/show/NCT043067055/30/2020100Recruiting
Drug: Tocilizumab|Other: Standard of care|Procedure: Continuous renal replacement therapy
Observational120
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
6/20/20203/13/20202/20/20203/17/2020
Tongji Hospital, Wuhan, Hubei, China
NCT04306705
79
https://ClinicalTrials.gov/show/NCT04322565Phase 25/30/202059Not yet recruitingDrug: ColchicineInterventional100Colchicine 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
6/30/20203/26/20204/1/20203/26/2020NCT04322565
80
https://ClinicalTrials.gov/show/NCT04293887Early Phase 15/30/202090Not yet recruitingDrug: Recombinant human interferon α1βInterventional328
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
6/30/20203/3/20203/1/20203/3/2020NCT04293887
81
https://ClinicalTrials.gov/show/NCT04321421Not Applicable5/31/202075
Active, not recruiting
Other: hyperimmune plasmaInterventional49Hyperimmune Plasma for Critical Patients With COVID-19COV19-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
5/31/20203/25/20203/17/20203/25/2020
Catherine Klersy, Pavia, PV, Italy
NCT04321421
82
https://ClinicalTrials.gov/show/NCT04324996
Phase 1|Phase 2
5/31/202071Recruiting
Biological: NK cells,IL15-NK cells,NKG2D CAR-NK cells,ACE2 CAR-NK cells,NKG2D-ACE2 CAR-NK cells
Interventional90
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
9/30/20203/27/20203/21/20203/27/2020
Chongqing Public Health Medical Center, Chongqing, China
NCT04324996
83
https://ClinicalTrials.gov/show/NCT04325906Not Applicable5/31/202055Not yet recruiting
Device: high flow nasal cannula (HFNC)|Procedure: Prone positioning (PP)
Interventional162
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
6/30/20203/30/20204/6/20203/30/2020
Rush University Medical Center, Chicago, Illinois, United States|Medical College of Wisconsin, Wauwatosa, Wisconsin, United States
NCT04325906
84
https://ClinicalTrials.gov/show/NCT043055745/31/202084RecruitingBehavioral: Use of social media during COVID-19Observational5000Social 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
5/31/20203/12/20203/8/20203/17/2020
Yale-NUS College, Singapore, Singapore
NCT04305574
85
https://ClinicalTrials.gov/show/NCT04261907Not Applicable5/31/2020114Not yet recruitingDrug: ASC09/ritonavir group|Drug: lopinavir/ritonavir groupInterventional160
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
6/30/20202/10/20202/7/20202/10/2020NCT04261907
86
https://ClinicalTrials.gov/show/NCT04276987Phase 15/31/2020106Not yet recruitingBiological: MSCs-derived exosomesInterventional30
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
7/31/20202/19/20202/15/20202/25/2020NCT04276987
87
https://ClinicalTrials.gov/show/NCT04318431Not Applicable6/1/202061Not yet recruitingDiagnostic Test: Data collection and rhinopharyngeal swabInterventional600
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
6/1/20203/24/20204/1/20203/26/2020
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/NCT043113986/1/202079Not yet recruiting
Diagnostic Test: New QIAstat-Dx fully automatic multiple PCR detection platform
Observational100
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
12/1/20203/17/20203/14/20203/17/2020
Huashan Hospital of Fudan University, Shanghai, Shanghai, China
NCT04311398
89
https://ClinicalTrials.gov/show/NCT04255017Phase 46/1/2020121Recruiting
Drug: Abidol hydrochloride|Drug: Oseltamivir|Drug: Lopinavir/ritonavir
Interventional400
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
7/1/20202/5/20202/1/20203/17/2020
Department and Institute of Infectious Disease, Wuhan, Hubei, China
NCT04255017
90
https://ClinicalTrials.gov/show/NCT04254874Phase 46/1/2020121Recruiting
Drug: Abidol hydrochloride|Drug: Abidol Hydrochloride combined with Interferon atomization
Interventional100
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
7/1/20202/5/20202/1/20203/17/2020
Department and Institute of Infectious Disease, Wuhan, Hubei, China
NCT04254874
91
https://ClinicalTrials.gov/show/NCT04263402Phase 46/1/2020121RecruitingDrug: MethylprednisoloneInterventional100
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
7/1/20202/10/20202/1/20203/17/2020
Department and Institute of Infectious Disease, Wuhan, Hubei, China
NCT04263402
92
https://ClinicalTrials.gov/show/NCT043246846/3/202061Not yet recruitingObservational198Prognostic Factors Keeping Track for Covid19 PneumoniaNIKE_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
6/30/20203/27/20204/3/20203/27/2020NCT04324684
93
https://ClinicalTrials.gov/show/NCT04304053Phase 36/15/202089Recruiting
Drug: Antiviral treatment and prophylaxis|Other: Standard Public Health measures
Interventional3040
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
6/15/20203/11/20203/18/20203/24/2020
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/NCT04285190Not Applicable6/15/2020110Not yet recruitingDrug: T89Interventional120
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
9/15/20202/26/20202/26/20202/26/2020NCT04285190
95
https://ClinicalTrials.gov/show/NCT04305106Not Applicable6/30/2020105RecruitingDrug: BevacizumabInterventional140
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
7/31/20203/12/20203/17/20203/26/2020
Qilu Hospital of Shandong University, Jinan, Shandong, China
NCT04305106
96
https://ClinicalTrials.gov/show/NCT04313322Phase 16/30/2020106RecruitingBiological: WJ-MSCsInterventional5
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
9/30/20203/18/20203/16/20203/18/2020
Stem Cells Arabia, Amman, Jordan
NCT04313322
97
https://ClinicalTrials.gov/show/NCT04273646Not Applicable6/30/2020135Not yet recruitingBiological: UC-MSCs|Drug: PlaceboInterventional48
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
2/15/20222/18/20202/16/20202/21/2020
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
6/30/202099RecruitingDrug: Escin|Drug: standard therapyInterventional120Escin in Patients With Covid-19 Infectionadd-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
8/30/20203/26/20203/23/20203/27/2020
Luca Gallelli, Catanzaro, Italy
NCT04322344
99
https://ClinicalTrials.gov/show/NCT043225136/30/202098RecruitingDiagnostic Test: Biomarkers expressionObservational110Biomarkers for Identification of SARS-COV-2 InfectionB-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
8/30/20203/26/20203/24/20203/27/2020
Luca Gallelli, Catanzaro, Italy
NCT04322513
100
https://ClinicalTrials.gov/show/NCT04280588Phase 27/1/2020130RecruitingDrug: Fingolimod 0.5 mgInterventional30Fingolimod 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
7/1/20202/21/20202/22/20202/21/2020
Wan-Jin Chen, Fuzhou, China
NCT04280588