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COVID-19 Seroprevalence in Pregnant Women and Blood Donors

Completed
Conditions
COVID-19 Respiratory Infection
Registration Number
NCT04893057
Lead Sponsor
Centre Hospitalier Universitaire de Besancon
Brief Summary

The study aims to measure the SARS-CoV-2 seroprevalence (ie. the proportion of people with antibodies against the virus) in pregnant women and blood donors in an administrative area of France, and to determine whether these measures are representative of the general population.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
797
Inclusion Criteria
  • Pregnant women

    • Adult female
    • Admitted to hospital for live birth
    • Informed consent
    • Affiliated to the French social security health insurance scheme
  • Blood donors

    • Adult male or female
    • Qualified for whole blood donation (up to 70 years old in France)
    • Informed consent
    • Affiliated to the French social security health insurance scheme
Exclusion Criteria
  • Legal incapacity or limited legal capacity
  • Subject without health insurance coverage
  • Exclusion period of another study or exclusion period of the French national healthy volunteer registry

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Anti-SARS-CoV-2 spike protein total IgGat inclusion

Total IgG directed against anti-SARS-CoV-2 spike protein as measured by ELISA assay

Secondary Outcome Measures
NameTimeMethod
Anti-SARS-CoV-2 nucleocapsid protein total IgGat inclusion

Total IgG directed against anti-SARS-CoV-2 nucleocapsid protein as measured by ELISA assay

Trial Locations

Locations (1)

CHU de besançon

🇫🇷

Besançon, France

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