CovidResearchTrials by Shray Alag


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COVID-19 convalescent hyperimmune plasmaWiki

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


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1634 Non-convalescent fresh frozen plasma (Standard plasma) Wiki 1.00

Correlated MeSH Terms (9)


Name (Synonyms) Correlation
D025241 Spondylarthritis NIH 1.00
D001167 Arteritis NIH 0.71
D012859 Sjogren's Syndrome NIH 0.71
D001327 Autoimmune Diseases NIH 0.58
D011111 Polymyalgia Rheumatica NIH 0.58
D013700 Giant Cell Arteritis NIH 0.58
D008180 Lupus Erythematosus, Systemic NIH 0.41
D001172 Arthritis, Rheumatoid NIH 0.38
D001168 Arthritis NIH 0.29

Correlated HPO Terms (5)


Name (Synonyms) Correlation
HP:0012089 Arteritis HPO 0.71
HP:0002960 Autoimmunity HPO 0.58
HP:0002725 Systemic lupus erythematosus HPO 0.41
HP:0001370 Rheumatoid arthritis HPO 0.38
HP:0001369 Arthritis HPO 0.29

There is one clinical trial.

Clinical Trials


1 Randomized, Open Label, Prospective Study of the Safety and Efficacy of Hyperimmune Convalescent Plasma in Moderate and Severe COVID-19 Disease

The clinical trial aims to study the safety and efficacy of transfusion of COVID-19 convalescent hyperimmune plasma for the treatment of moderate and severe forms of COVID-19 disease in comparison with non-convalescent fresh frozen plasma (standard plasma).

NCT04392414 COVID-19 Biological: COVID-19 convalescent hyperimmune plasma Biological: Non-convalescent fresh frozen plasma (Standard plasma)

Primary Outcomes

Description: The number and proportion of patients with the normal body temperature (≤37.2 C) at the days 1, 2, 3, 4, 5, 6, 7 after the start of therapy, for the statistical data comparison between the two arms.

Measure: The number and proportion of patients with the normal body temperature (≤37.2 C) at the day 1, 2, 3, 4, 5, 6, 7 after the start of therapy

Time: Days 1, 2, 3, 4, 5, 6, 7

Secondary Outcomes

Description: For each patient, the number of days passed from the plasma administration to placing on mechanical ventilation will be noted, for the statistical data comparison between the two arms.

Measure: Days before mechanical ventilation

Time: 30 days

Description: For each patient, the number of days he or she spent on the oxygen support after the plasma administration will be noted, for the statistical data comparison between the two arms.

Measure: Days of need for oxygen therapy

Time: 30 days

Description: For each patient, the entire duration of ICU stay after the plasma administration will be noted, for the statistical data comparison between the two arms.

Measure: Days of stay in the ICU

Time: 30 days

Description: For each patient, the entire duration of hospital stay after the plasma administration will be noted, for the statistical data comparison between the two arms.

Measure: Days of hospitalization

Time: 30 days

Description: Changes of the plasma levels of the SARS-CoV-2 antibodies, days 14 and 30 after the treatment start vs those levels before the treatment start (day 0) for the same patients.

Measure: Changes of the titer of the SARS-CoV-2 antibodies in the blood plasma of patients

Time: Days 0, 14, 30

Description: Changes of the plasma levels of IL2, IL6, IL10, TNFalpha and INFgamma, days 3 and 7 after the treatment start vs those levels before the treatment start (day 0) for the same patients.

Measure: Dynamics of the cytokine profile

Time: Days 0, 3, 7

Description: Incidence of administering IL6 receptor blockers (tocilizumab, sarilumab)

Measure: Incidence of the cytokine storm development and the need of administering cytokine storm inhibitors

Time: Days 3, 7

Description: Changes of the plasma levels of C-reactive protein, days 1, 2, 3, 4, 5, 6, 7 after the treatment start vs those levels before the treatment start (Day 0) for the same patients.

Measure: Dynamics of the level of C-reactive protein

Time: Days 0, 1, 2, 3, 4, 5, 6, 7

Description: 30-day mortality rate, for the statistical data comparison between the two arms.

Measure: 30-day mortality rate

Time: 30 days


No related HPO nodes (Using clinical trials)