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Convalescent Plasma (CP)Wiki

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


Correlated Drug Terms (4)


Name (Synonyms) Correlation
drug931 Drugs and supportive care Wiki 0.71
drug2363 Radspherin Wiki 0.71
drug2676 Standard COVID-19 therapies Wiki 0.71
drug3362 nasopharyngeal Covid 19 RT-PCR Wiki 0.71

Correlated MeSH Terms (5)


Name (Synonyms) Correlation
D000077216 Carcinoma, Ovarian Epithelial NIH 0.71
D010534 Peritoneal Neoplasms NIH 0.71
D006528 Carcinoma, Hepatocellular NIH 0.71
D002277 Carcinoma NIH 0.63
D010051 Ovarian Neoplasms NIH 0.50

Correlated HPO Terms (3)


Name (Synonyms) Correlation
HP:0001402 Hepatocellular carcinoma HPO 0.71
HP:0030731 Carcinoma HPO 0.63
HP:0100615 Ovarian neoplasm HPO 0.50

There are 2 clinical trials

Clinical Trials


1 Convalescent Plasma to Optimize Treatment of COVID-19 Disease in Pediatric Patients: A Feasibility Study

COVID-19 is increasingly affecting children but convalescent plasma (CP) has not been adequately studied in children to date. The study will determine safety of convalescent plasma for pediatric patients with severe, or at high risk for severe, COVID-19 disease.

NCT04458363 COVID Biological: Convalescent Plasma (CP) Drug: Standard COVID-19 therapies

Primary Outcomes

Description: Safety of convalescent plasma for pediatric patients will be determined by capturing the grade 3-5 adverse events that are possible, probably or definitely related to the CP infusion, defined using the NCI Common Terminology Criteria for Adverse Events (CTCAE)

Measure: Number of grade 3-5 adverse events that are possible, probably or definitely related to the convalescent plasma (CP) infusion

Time: 28 days

Secondary Outcomes

Description: Change in percent of supplemental oxygen within 72 hours after infusion

Measure: Change in percent of supplemental oxygen

Time: Baseline, 72 hours after infusion

Description: Number of patients that required change in level of respiratory support such as nasal canula, non-invasive ventilation, mechanical ventilation, high frequency oscillator ventilation, and extracorporeal membrane oxygenation (ECMO)

Measure: Number of patients that required change in level of respiratory support

Time: Baseline, 72 hours after infusion

Description: Number of deaths

Measure: Mortality

Time: up to 1 year

Description: Length of ICU stay (days) will be recorded

Measure: Mean length of ICU stay (days)

Time: Up to 28 days

Description: Length of hospital stay (days) will be recorded

Measure: Mean length of hospital stay (days)

Time: Up to 28 days

Description: Length of ventilation (days) will be recorded

Measure: Mean length of ventilation (days)

Time: Up to 28 days

Description: Number of patients with progression to renal dysfunction and/or multisystem organ failure will be recorded

Measure: Number of patients with progression to renal dysfunction and/or multisystem organ failure

Time: up to 1 year

Description: Cytokine milieu will be assayed by Luminex

Measure: IL-6 level

Time: up to 28 days

Description: Cellular studies will be used for evaluation of anti-SARS CoV 2 specific T cells

Measure: Number of anti-SARS CoV 2 specific T cells

Time: up to 28 days

Description: Cellular studies will be used for evaluation of diversity of circulating T cells

Measure: Diversity of circulating T cells

Time: up to 28 days

Description: Antibody titers to SARS-CoV-2 evaluation will be performed in vivo

Measure: ARS-CoV-2 Antibody Titer

Time: up to 28 days

Description: Neutralizing antibodies are a type of virus specific antibody that not only bind virus but bind in a manner that prevents viral infection. Test will be will be performed in vivo.

Measure: SARS-CoV-2 Neutralizing Titer

Time: up to 28 days

2 Convalescent Plasma Treatment in COVID-19 Patients at a Tertiary Care Center in Pakistan

The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) occurred initially in December 2019 in the city of Wuhan, Hubei province, China. Patients mainly presented with respiratory symptoms and this novel pathogen was identified.At present, the core management of COVID-19 includes infection prevention, case detection, monitoring, and supportive care. While specific new drugs and vaccines are being researched, certain drugs that are already present in medical arsenal are under trial too. One investigational treatment being explored for COVID-19 is the use of convalescent plasma (CP) collected from recovered COVID-19 patients. Convalescent Plasma is a source of passive immune therapy- the administration of specific antibodies against a given agent for preventing or treating an infectious disease due to that agent. The main anticipated mechanism of action of Convalescent Plasma therapy in COVID19 is viral neutralization. Other possible mechanisms include antibody-dependent cellular cytotoxicity and phagocytosis. There are numerous examples in which convalescent plasma (CP) has been used successfully as post exposure prophylaxis and/or treatment of infectious diseases, including other outbreaks of coronaviruses e.g. SARS-1, MERS-CoV and very recently in 2014, the Ebola virus outbreak. In SARS-CoV-2, Shen et al published a case series of 5 critically ill patients with COVID-19 and acute respiratory distress syndrome showing improvement in clinical status after transfusion of CP. Therefore, the objective of this study is to determine the safety and efficacy of transfusing convalescent plasma in patients admitted with COVID-19 at Aga Khan University Karachi, Pakistan. The investigators hypothesize that CP will decrease the length of hospital stay and overall mortality in patients with COVID-19. In this study, convalescent plasma will be collected from the donors who have been recovered from SARS-CoV-2 infection and transfused it to the patients admitted with active severe /critical COVID-19 at the Aga Khan University Hospital Karachi. STUDY DESIGN: Non-randomized open Label trial INCLUSION CRITERIA IN TREATMENT ARM: i. Inpatients at AKU with positive SARS-CoV-2 infection by rRT-PCR and who have provided written informed consent for inclusion in the trial; ii. Age ≥ 18 years; iii. Severe or immediately life-threatening COVID-19 defined by any of: - Respiratory rate ≥ 30/min; - Blood oxygen saturation ≤ 93% at room air; - Partial pressure of arterial Oxygen to Fraction of inspired Oxygen ratio < 300; - Lung infiltrates > 50% within 24 to 48 hours on radiology ( X-ray or CT scan); - Need for mechanical ventilation. - respiratory failure - septic shock - multiple organ dysfunction or failure EXCLUSION CRITERIA: i. Negative rRT-PCR from respiratory secretions or blood within 48 h prior to assessment of eligibility. ii. History of allergic reaction to blood or plasma products (as judged by the investigator). iii. Medical conditions in which receipt of 500 mL intravascular volume may be detrimental to the patient (e.g., actively decompensated congestive heart failure). iv. Enrolment in any other clinical trial for an investigational therapy. CONTROL GROUP: COVID-19 patients recruited during the period before CP becomes available or for whom no compatible CP is available will be given Standard of Care and will be followed for study outcomes. Data from these SC patients will be used as comparator in the analysis of the study.

NCT04476888 Covid19 Biological: Convalescent Plasma (CP) Other: Drugs and supportive care

Primary Outcomes

Description: Decrease length of stay in hospital , Decrease length of stay in ICU/special care unit

Measure: Decrease length of stay

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Status alive or death

Measure: Overall mortality

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Any adverse event after the transfusion of Convalescent plasma which include TRALI, TACO, allergic reaction, anaphylaxis.

Measure: Incidence of adverse events related to Convalescent Plasma transfusion

Time: After receiving intervention (CP) till 24 hours

Secondary Outcomes

Description: Modified from WHO scale. It includes clinical status of patient in terms of respiratory support needed.

Measure: Ordinal scale

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in serum ferritin levels after intervention

Measure: Improvement in Laboratory Parameters: Serum Ferritin

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in serum Procalcitonin levels after intervention

Measure: Improvement in Laboratory Parameters: Procalcitonin

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in C-Reactive protein levels after intervention

Measure: Improvement in Laboratory Parameters: C-Reactive Protein

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in D-Dimer levels after intervention

Measure: Improvement in Laboratory Parameters: D-Dimer

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in complete blood count after intervention

Measure: Improvement in Laboratory Parameters: Complete Blood count

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month

Description: Time to improvement in chest X-Ray findings after intervention

Measure: Chest X-Ray findings

Time: From date on which intervention given until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 1 month


No related HPO nodes (Using clinical trials)