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COVID-19 Seroprevalence in Pregnant Women and Blood Donors (CoVERED)

C

Centre Hospitalier Universitaire de Besancon

Status

Completed

Conditions

COVID-19 Respiratory Infection

Study type

Observational

Funder types

Other

Identifiers

NCT04893057
2021/601

Details and patient eligibility

About

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.

Enrollment

797 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

797 participants in 2 patient groups

Pregnant women
Description:
Women admitted to hospital for a live birth.
Blood donors
Description:
Subjects qualified for whole blood donation

Trial contacts and locations

1

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Central trial contact

Noémie Nminej

Data sourced from clinicaltrials.gov

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