CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Lopinavir-Ritonavir Drug CombinationWiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug343 Bevacizumab Injection Wiki 0.71
drug2300 Standard Care Wiki 0.50

Correlated MeSH Terms (3)


Name (Synonyms) Correlation
D011014 Pneumonia NIH 0.06
D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.06

There is one clinical trial.

Clinical Trials


1 Evaluation of Additional Treatments for COVID-19: a Randomized Trial in Niger

The purpose of this study is to assess whether lopinavir/ritonavir (or eventually other antiviral drugs) is effective at reducing the rate of hospitalization among confirmed COVID-19 cases treated as outpatients.

NCT04409483 Covid-19 Drug: Lopinavir-Ritonavir Drug Combination Combination Product: Standard Care

Primary Outcomes

Description: Hospitalization associated with desaturation (SpO2 ≤92%) or death due to any cause

Measure: Hospitalization or death

Time: 15 days following randomization

Secondary Outcomes

Description: Death due to any cause

Measure: All-cause mortality

Time: 15 days following randomization

Description: Death due to any cause

Measure: All-cause mortality

Time: 28 days following randomization

Description: Length of time between randomization and hospitalization associated with desaturation (SpO2 ≤92%)

Measure: Time to hospitalization

Time: 28 days following randomization

Description: Total duration of hospitalization associated with desaturation (SpO2 ≤92%)

Measure: Length of hospitalization

Time: 28 days following randomization

Description: Proportion of participants admitted to an intensive care unit

Measure: Admission to intensive care

Time: 28 days following randomization

Description: Proportion of participants having an adverse event

Measure: Adverse events

Time: 28 days following randomization

Description: Proportion of participants having a serious adverse event

Measure: Serious adverse events

Time: 28 days following randomization


No related HPO nodes (Using clinical trials)