CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


ArbidolWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug1363 Lopinavir and Ritonavir Tablets Wiki 0.71
drug2753 basic treatment Wiki 0.50
drug2114 Routine care for COVID-19 patients Wiki 0.50
drug923 Favipiravir Wiki 0.17
drug1086 Hydroxychloroquine Wiki 0.07

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D003141 Communicable Diseases NIH 0.06
D011014 Pneumonia NIH 0.04
D007239 Infection NIH 0.04
D045169 Severe Acute Respiratory Syndrome NIH 0.04
D018352 Coronavirus Infections NIH 0.03

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.04

There are 2 clinical trials

Clinical Trials


1 A Randomized, Open-label, Controlled Study of the Efficacy of Lopinavir Plus Ritonavir and Arbidol for Treating With Patients With Novel Coronavirus Infection

The study explores the efficacy of lopinavir plus ritonavir and arbidol in treating with novel coronavirus infection. As a result this study would provide evidence for the clinical usage of these drugs in the future .

NCT04252885 Coronavirus Infections Drug: Lopinavir and Ritonavir Tablets Drug: Arbidol
MeSH:Infection Communicable Diseases Coronavirus Infections Severe Acute Respiratory Syndrome

Primary Outcomes

Description: Novel coronaviral nucleic acid is measured in nose / throat swab at each time point.

Measure: The rate of virus inhibition

Time: Day 0, 2, 4, 7, 10, 14 and 21

Secondary Outcomes

Description: Body temperature will be followed everyday during time frame.

Measure: The disease prorogation-temperature

Time: Day 0 till day 21

Description: Respiratory rate will be followed everyday during time frame.

Measure: The disease prorogation-respiratory function 1

Time: Day 0 till day 21

Description: Oxygen saturation of blood will be followed everyday during time frame.

Measure: The disease prorogation-respiratory function 2

Time: Day 0 till day 21

Description: Chest imaging will be taken at each time point.

Measure: The disease prorogation-respiratory function 3

Time: Day 0, 4, 7, 10, 14 and 21

Other Outcomes

Description: Blood pressure and heart rate will be followed everyday during time frame.

Measure: Patients health condition-routine test

Time: Day 0 till day 21

Description: Liver function will be assessed as AST, ALT and TBIL at each time point.

Measure: Patients health condition-liver function

Time: Day 0, 4, 7, 10, 14 and 21

Description: Kidney function will be assessed as eGFR and creatine clearance rate at each time point.

Measure: Patients health condition-kidney function

Time: Day 0, 4, 7, 10, 14 and 21

Description: Blood routine and myocardial enzyme will be measured at each time point.

Measure: Patients health condition-other blood routine test

Time: Day 0, 4, 7, 10, 14 and 21

Description: Flow cytometry classification and counting and cytokines will be measured at each time point.

Measure: Patients health condition-blood routine test

Time: Day 0, 4, 7, 10, 14 and 21

2 Randomized, Open, Multicenter Study on the Efficacy and Safety of Arbidol Hydrochloride Tablets in Treating Pneumonia in Patients Infected With Novel Coronavirus (2019-ncov).

In the absence of 2019-ncov specific therapeutic drugs, arbidol is effective against a variety of coronaviruses in vitro pharmacodynamics. In order to observe the efficacy and safety of arbidol in the treatment of 2019-ncov infected pneumonia, this study is planned.

NCT04260594 2019-nCoV Drug: Arbidol Other: basic treatment
MeSH:Pneumonia
HPO:Pneumonia

Primary Outcomes

Measure: Virus negative conversion rate in the first week

Time: first week

Secondary Outcomes

Description: virus negative conversion rate in second week, overall virus negative conversion rate

Measure: Virus negative conversion rate

Time: 14-20 days

Description: defined as: the rate of Axillary temperature ≤37.5 ℃ for at least 48h

Measure: Antipyretic rate

Time: 14-20 days

Description: time to relieve symptoms of fever, cough, dyspnea, myalgia, etc

Measure: Symptom relief time

Time: 14-20 days

Description: no adjuvant oxygen therapy, resting oxygen saturation>95%, oxygenation index>350

Measure: Finger oxygen improvement rate

Time: 14-20 days

Description: Mild, common type progression to severe or critical illness rate

Measure: Disease progression rate

Time: 14-20 days

Measure: Mortality rate

Time: 14-20 days

Measure: Incidence of severe adverse reactions

Time: 14-20 days

Measure: Change curve of peripheral blood lymphocyte count

Time: 14-20 days


Related HPO nodes (Using clinical trials)