CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


plasma therapy using convalescent plasma with antibody against SARS-CoV-2Wiki

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


Correlated Drug Terms (2)


Name (Synonyms) Correlation
drug1062 High-Titer Anti-SARS-CoV-2 (COVID 19) Convalescent Plasma Wiki 1.00
drug2114 Routine care for COVID-19 patients Wiki 0.71

Correlated MeSH Terms (4)


Name (Synonyms) Correlation
D011014 Pneumonia NIH 0.06
D007239 Infection 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 Use of Convalescent Plasma Therapy for COVID-19 Patients With Hypoxia: a Prospective Randomized Trial

Plasma therapy using convalescent plasma has been shown to be effective in severe acute respiratory syndrome, Ebola virus infection and in H1N1 influenza. More recently there has been a report of the use of convalescent plasma in the treatment of 5 ventilated COVID-19 patients with the suggestion of expedited recovery as the patients improved 1 week after the transfusion. However, this was not a clinical trial and the patients were on other antiviral medication.; therefore, there is a need to undertake such a trial to see if deploying plasma with SARS-CoV-2 neutralizing antibody has utility in managing patients infected with COVID-19 in respiratory distress. The objective of this pilot study is to compare plasma therapy using convalescent plasma with antibody against SARS-CoV-2 to usual supportive therapy in COVID-19 patients with pneumonia and hypoxia, and to determine if the clinical course is improved. The difference between groups will allow an effect size to be determined for a definitive clinical trial.

NCT04356534 SARS-CoV 2 COVID-19 Other: plasma therapy using convalescent plasma with antibody against SARS-CoV-2 Other: Routine care for COVID-19 patients

Primary Outcomes

Description: Could the plasma therapy avoid or delay the need for invasive ventilation

Measure: Requirement for invasive ventilation

Time: through study completion up to 28 days

Secondary Outcomes

Description: Through the use of CT values

Measure: Change in viral clearance

Time: through study completion up to 28 days

Description: Chest Xray

Measure: Radiological change

Time: through study completion up to 28 days

Description: As a measure of a change in inflammation

Measure: Change in white cell count

Time: through study completion up to 28 days

Description: A change in C reactive protein as a measure of a change in inflammation

Measure: C reactive protein measurement

Time: through study completion up to 28 days

Description: A change in lactate dehydrogenase as a measure of an improvement in the severity of the disease process

Measure: lactate dehydrogenase measurement

Time: through study completion up to 28 days

Description: A change in procalcitonin as a measure of an improvement in the severity of the disease process

Measure: Procalcitonin measurement

Time: through study completion up to 28 days

Description: A change in D Dimer as a measure of an improvement in the severity of the disease process

Measure: D Dimer measurement

Time: through study completion up to 28 days

Description: A change in Ferritin as a measure of an improvement in the severity of the disease process

Measure: Ferritin measurement

Time: through study completion up to 28 days

Description: A change in troponin T as a measure of an improvement in the severity of the disease process

Measure: Troponin T measurement

Time: through study completion up to 28 days

Description: A change in brain naturetic peptide as a measure of an improvement in the severity of the disease process

Measure: Brain naturetic peptide measurement

Time: through study completion up to 28 days

Description: Mortality rate due to COVID-19

Measure: Mortality rate

Time: Up to 28 days of the study


No related HPO nodes (Using clinical trials)