Trials / Completed
CompletedNCT04397523
Efficacy and Safety of COVID-19 Convalescent Plasma
Use of COVID-19 Convalescent Plasma in the Patients Infected With COVID-19 (SARS-CoV-2) - Efficacy and Safety
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Institute for Transfusion Medicine of RNM · Other Government
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
Administration of convalescent plasma obtained from donors with prior documented SARS-CoV-2 infection
Detailed description
There are currently no proven therapeutic options for coronavirus disease (COVID-19), the infection caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Human convalescent plasma is an option for treatment of COVID-19. Experience from prior outbreaks with other coronaviruses, such as SARS-CoV-1, MERS and H1N1 shows that convalescent plasma can be effective. Convalescent plasma will be obtained by plasmapheresis or regular whole blood donation in subjects who recovered from COVID-19 and who are otherwise eligible for donation according to the Institutional protocol. Recipients will be COVID-19 patients requiring hospitalization. A blood-type matched transfusion of convalescent plasma will be infused and recipients will be followed up.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | anti-SARS-CoV-2 convalescent plasma | Administration of convalescent plasma obtained from donors with prior documented SARS-CoV-2 infection |
Timeline
- Start date
- 2020-04-30
- Primary completion
- 2021-05-10
- Completion
- 2021-05-10
- First posted
- 2020-05-21
- Last updated
- 2024-05-28
- Results posted
- 2024-05-28
Locations
1 site across 1 country: North Macedonia
Source: ClinicalTrials.gov record NCT04397523. Inclusion in this directory is not an endorsement.