Convalescent Plasma in Hospitalized COVID-19 Patients

NCT05157165 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2023-07-21

No results posted yet for this study

Summary

The study assesses the efficacy and safety of administration of hyperimmune plasma in hospitalized COVID-19 patients. Efficacy was measured as 28-day mortality following convalescent plasma transfusion. Safety was measured as the rate of adverse reactions. to plasma infusion.

Conditions

Interventions

BIOLOGICAL

Convalescent plasma

Hyperimmune plasma from convalescent COVID-19 donors with titre 1:80 or more

Sponsors & Collaborators

  • Azienda Socio Sanitaria Territoriale di Mantova

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05157165 on ClinicalTrials.gov