CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Plasma from a volunteer donorWiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug1184 SARS-CoV-2 convalescent plasma Wiki 0.58
drug335 Colchicine Wiki 0.41

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D011024 Pneumonia, Viral NIH 0.14
D011014 Pneumonia NIH 0.07
D045169 Severe Acute Respiratory Syndrome NIH 0.06
D018352 Coronavirus Infections NIH 0.05

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002090 Pneumonia HPO 0.07

There is one clinical trial.

Clinical Trials


1 Comparison of the Efficacy and Safety of Human Coronavirus Immune Plasma (HCIP) vs. Control (SARS-CoV-2 Non-immune) Plasma Among Outpatients With Symptomatic COVID-19.

To assess the efficacy and safety of Human coronavirus immune plasma (HCIP) to reduce the risk of hospitalization or death, the duration of symptoms and duration of nasopharyngeal or oropharyngeal viral shedding.

NCT04373460 SARS-CoV 2 Biological: SARS-CoV-2 convalescent plasma Biological: Plasma from a volunteer donor

Primary Outcomes

Description: Cumulative incidence measured as the proportion of subjects who were hospitalized or who died prior to hospitalization

Measure: Cumulative incidence of hospitalization or death prior to hospitalization

Time: Up to day 28

Description: Cumulative incidence measured as the proportion of subjects experiencing an Serious Adverse Event (SAE).

Measure: Cumulative incidence of treatment-related serious adverse events

Time: Up to day 28

Description: Cumulative incidence measured as the proportion of subjects experiencing a Grade 3 or higher.

Measure: Cumulative incidence of treatment-related grade 3 or higher adverse events

Time: Up to day 90

Secondary Outcomes

Description: Analysis of serum SARS-CoV-2 antibody titers will also primarily be descriptive, comparing the geometric mean titers at day 0, 14, 28 and 90 between the randomized arms and calculating the shift or change in the titer distribution.

Measure: Change in serum SARS-CoV-2 antibody titers

Time: Days 0, 14, 28 and 90

Description: Duration in days of SARS-CoV-2 PCR time to negativity will be analyzed by calculating the number of days taken for a positive participant to lose positivity from day 0 to day 28.

Measure: Time to SARS-CoV-2 Polymerase Chain Reaction (PCR) negativity

Time: Up to day 28

Other Outcomes

Description: Change in levels of SARS-CoV-2 RNA between randomized arms from Day 0 to Day 28.

Measure: Change in level of SARS-CoV-2 RNA

Time: Day 0 to Day 28

Description: Comparison of participant self-assessed blood oxygen saturation levels (in percentage oxygen) between treatment arms using pulse oximetry from Day 0 to Day 28.

Measure: Change in oxygen saturation levels

Time: Day 0 to Day 28

Description: Secondary infection will be assessed by measuring the number of individuals that live in the same house as the active arm who became sick by the end of follow-up period.

Measure: Rate of participant-reported secondary infection of housemates

Time: Up to day 90

Description: Disease severity measured by time (in days) to admission to the ICU or , invasive mechanical ventilation or time to death.

Measure: Time to ICU admission, invasive mechanical ventilation or death in hospital

Time: Up to day 90

Description: Time (in days) to resolution of COVID-19 symptoms will be based on temperature logs and symptom score sheets.

Measure: Time to resolution of COVID-19 symptoms

Time: Up to day 90

Description: Assess change in hospitalization rate as measured by number of hospitalizations stratified by age groups <65 and >=65

Measure: Impact of convalescent plasma on outcome as assessed by change in hospitalization rate

Time: Day 0 to Day 90

Description: Impact of donor antibody titers (high/low) will be assessed by hospitalization rate as measured by number of hospitalizations.

Measure: Impact of donor antibody titers on hospitalizaton rate of convalescent plasma recipients

Time: Day 0 to Day 90

Description: Impact of donor antibody titers (high/low) will be assessed by antibody levels

Measure: Impact of donor antibody titers on antibody levels of convalescent plasma recipients

Time: Day 0 to Day 90

Description: Impact of donor antibody titers (high/low) will be assessed by viral positivity rates (number of SARS-CoV-2 positive cases per total cases)

Measure: Impact of donor antibody titers on viral positivity rates of convalescent plasma recipients

Time: Day 0 to Day 90


No related HPO nodes (Using clinical trials)