CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


SildenafilWiki

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


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug2122 Placebo Wiki 0.05

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D007239 Infection NIH 0.05

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Sildenafil for Treating Patients With COVID-19 and Perfusion Mismatch: A Pilot Randomised Trial

This randomised trial aims to assess the role of sildenafil in improving oxygenation amongst hospitalised patients with COVID19.

NCT04489446 Covid19 SARS-COV2 Infection Drug: Sildenafil Drug: Placebo
MeSH:Infection

Primary Outcomes

Description: Mean difference in alveolar oxygen pressure to inspired oxygen fraction (Pa/Fi) ratios.

Measure: Arterial Oxygenation

Time: One hour after sildenafil administration

Description: Mean difference in alveolar oxygen pressure to inspired oxygen fraction (Pa/Fi) ratios.

Measure: Arterial Oxygenation

Time: Daily until the end of follow-up (up to 15 days after randomisation)

Description: Mean difference in the alveolo-arterial gradient between study groups.

Measure: Alveolo-arterial gradient

Time: One hour after sildenafil administration

Description: Mean difference in the alveolo-arterial gradient between study groups.

Measure: Alveolo-arterial gradient

Time: Daily until the end of follow-up (up to 15 days after randomisation)

Secondary Outcomes

Description: Proportion of patients requiring admission to an intensive care unit in each study group

Measure: Intensive care unit admission

Time: Up to two weeks after randomisation

Description: Proportion of patients requiring noninvasive mechanical ventilation o high-flow nasal cannula unit in each study group

Measure: Noninvasive Mechanical Ventilation or Requirement of High-Flow Nasal Cannula

Time: Up to two weeks after randomisation

Description: Proportion of patients requiring invasive mechanical ventilation in each study group

Measure: Invasive mechanical ventilation

Time: Up to two weeks after randomisation

Description: Proportion of patients that survived COVID19 in each study group

Measure: Survival

Time: Up to two weeks after randomisation

Other Outcomes

Description: Adverse events attributable to sildenafil use.

Measure: Adverse events

Time: Up to two weeks after randomisation


No related HPO nodes (Using clinical trials)