CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Diagnostic Laboratory Biomarker AnalysisWiki

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


Correlated Drug Terms (5)


Name (Synonyms) Correlation
drug2852 Telemedicine follow-up visit Wiki 1.00
drug1400 In-person in clinic follow-up visit Wiki 1.00
drug983 Electronic Health Record Review Wiki 1.00
drug424 Biospecimen Collection Wiki 0.58
drug2312 Questionnaire Administration Wiki 0.38

Correlated MeSH Terms (2)


Name (Synonyms) Correlation
D003141 Communicable Diseases NIH 0.08
D007239 Infection NIH 0.05

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 Evaluation of Coronavirus Disease 19 (COVID-19) Convalescent Plasma

This study investigates convalescent plasma (CCP) collected from the blood of patients who have recovered from COVID-19 before use in treating patients with current COVID-19 infection. "Convalescent plasma" means that the plasma is coming from someone who has recovered from a COVID-19 infection. There may be antibodies present in CCP, that targets SARS-CoV-2, the virus responsible for COVID-19. The purpose of this study is to learn more about COVID-19 convalescent plasma and the effect it may have in treating COVID-19 infection.

NCT04497779 Asymptomatic COVID-19 Infection Laboratory-Confirmed Symptomatic COVID-19 Infection Laboratory-Confirmed Procedure: Biospecimen Collection Other: Diagnostic Laboratory Biomarker Analysis Other: Electronic Health Record Review Other: Questionnaire Administration
MeSH:Infection Communicable Diseases Laboratory Infection

Primary Outcomes

Description: Will be assayed for severe acute respiratory syndrome (SARS‐CoV‐2) immunoassay, coronavirus (CoV) PepSeq assay, and SARS‐CoV‐2 lenti‐based neutralizing antibody titer.

Measure: Convalescent plasma (CCP) units infused in coronavirus disease-2019 (COVID-19) patients

Time: Up to 12 months after enrollment

Description: Will naturally be compared to reported data from the other studies. Analysis will focus on demonstrating that the antibody content of donor plasma increases the odds of surviving past day 28. Will also develop a nomogram for the probability of success (alive at day 28), accounting for patient, donor material and donor antibody characteristics measurable covariates.

Measure: All-cause mortality

Time: At day 28 post-CCP infusion

Description: Will be examined to see how this relates to the duration of hospitalization.

Measure: Donor antibody levels

Time: Up to 28 days post-CCP infusion

Secondary Outcomes

Description: Will be assessed on a 7-point ordinal scale, as recommended by the WHO patient outcome R&D Blueprint Group.

Measure: Incidence of adverse events

Time: Up to 28 days post-CCP infusion

Description: Will be assessed on a 7-point ordinal scale. The scale is as follows: Death; Hospitalized, on invasive mechanical ventilation or ECMO; Hospitalized, on non-invasive ventilation or high flow oxygen devices; Hospitalized, requiring low flow supplemental oxygen; Hospitalized, not requiring supplemental oxygen - requiring ongoing medical care (COVID-19 related or otherwise); Hospitalized, not requiring supplemental oxygen - no longer requires ongoing medical care (other than per protocol RDV administration); Not hospitalized

Measure: CCP recipient outcomes

Time: Up to 28 days post-CCP infusion

Other Outcomes

Description: Patient can stay at the hospital for up to 28 days post-CCP infusion

Measure: Duration of hospitalization (days)

Time: Up to 28 days post-CCP infusion

Description: Will be assessed on a 7-point ordinal scale.

Measure: Time to clinical improvement (days)

Time: Up to 28 days post-CCP infusion


No related HPO nodes (Using clinical trials)