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Covid-19 Convalescent Plasma and Monoclonal Antibodies Treatment of Immunocompromised Patients (Covid-IC)

U

University Hospital, Strasbourg, France

Status

Enrolling

Conditions

COVID-19 Convalescent Plasma Treatment

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Data on the use of convalescent plasma in the treatment of covid-19 are scarce: the results of randomized studies involving mainly immunocompetent patients are disappointing, while case series or retrospective data on more selected patients , in particular immunocompromised patients suggest a benefit in these patients whose clinical manifestation seems essentially related to the uncontrolled infection and not the cytokine storm.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patient
  • Immunocompromised patient (solid neoplasia, malignant hemopathy, solid organ transplantation, primary immune deficiency, systemic disease, chronic inflammatory disease, etc.)
  • Hospitalized between 25/02/2020 and 15/01/2023 at HUS, ICANS, CH Colmar and CH Mulhouse
  • Having received curative monoclonal antibody treatment or convalescent plasma treatment for SARS-Cov2 infection
  • Patient who has not expressed, after being informed, his opposition to the reuse of his data for scientific research purposes.

Exclusion criteria

  • Subject who expressed their opposition to participating in the study
  • Subject under guardianship, curatorship or safeguard of justice

Trial contacts and locations

1

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Central trial contact

François DANION, MD

Data sourced from clinicaltrials.gov

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