CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


basic treatmentWiki

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


Correlated Drug Terms (4)


Name (Synonyms) Correlation
drug289 Equipment with smartwatch throughout hospital stay on the general ward Wiki 0.71
drug974 lopinavir/ritonavir tablets or Arbidol or chloroquine phosphate Wiki 0.71
drug177 Carrimycin Wiki 0.71
drug58 Arbidol Wiki 0.50

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D003141 Communicable Diseases NIH 0.08
D011014 Pneumonia NIH 0.06
D007239 Infection NIH 0.06
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.11

There are 2 clinical trials

Clinical Trials


1 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

2 The Efficacy and Safety of Carrimycin Treatment in Patients With Novel Coronavirus Infectious Disease (COVID-19) : A Multicenter, Randomized, Open-controlled Study

The novel coronavirus infectious disease ( COVID-19") induced by novel coronavirus(SARS-CoV-2) in December 2019 has outbreaked in Wuhan. It may lead to epidemic risk in global. As the COVID-19 is an emerging infectious disease, it has not scientifically recognized and has no effective drugs for treatment currently. Therefore, we will launch a scientific project "The efficacy and safety of carrimycin treatment in 520 patients with COVID-19 stratificated clinically: A multicenter, randomized (1:1), open-controlled (one of lopinavir/ritonavir tablets or Arbidol or chloroquine phosphate) study" . We try to establish the criteria for clinical cure and the early predictive model of COVID-19 progression. The primary efficiency outcomes were:(1) Fever to normal time (day); (2) Pulmonary inflammation resolution time (HRCT) (day); and (3)Negative conversion (%) of SARS-CoV-2 RNA at the end of treatment. The secondary efficiency outcomes and adverse events were observed.

NCT04286503 Novel Coronavirus Infectious Disease (COVID-19) Drug: Carrimycin Drug: lopinavir/ritonavir tablets or Arbidol or chloroquine phosphate Drug: basic treatment
MeSH:Communicable Diseases Infection Coronavirus Infections

Primary Outcomes

Description: Fever to normal time (day)

Measure: Fever to normal time (day)

Time: 30 days

Description: Pulmonary inflammation resolution time (HRCT) (day)

Measure: Pulmonary inflammation resolution time (HRCT) (day)

Time: 30 days

Description: Negative conversion (%) of 2019-nCOVRNA in gargle (throat swabs) at the end of treatment

Measure: Negative conversion (%) of 2019-nCOVRNA in gargle (throat swabs) at the end of treatment

Time: 30 days


Related HPO nodes (Using clinical trials)