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Clinical Trials/NCT04816084
NCT04816084CompletedNot Applicable

SERUR : Etude sérologique COVID-19 (Anti-SARS CoV 2) du Personnel de l'Université de Reims Champagne-Ardenne

Université de Reims Champagne-Ardenne1 site in 1 country389 target enrollmentStarted: November 5, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
389
Locations
1
Primary Endpoint
Prevalence of IgG and IgM anti-SARS CoV2 antibodies

Study Overview

Brief Summary

This study was designed to determine, in a screening situation within the framework of university preventive medicine, the prevalence of positive anti-SARS-Cov 2 serology among the staff of the University of Reims Champagne-Ardenne. The serological tests chosen will allow systematic detection of anti-SARS-CoV-2 IgM and anti-SARS-Cov-2 IgG to assess the moment of potential contamination prior to resumption of occupational activity.

Detailed Description

Objective:

This study was designed to determine, in a screening situation within the framework of university preventive medicine, the prevalence of positive anti-SARS-Cov 2 serology among the staff of the University of Reims Champagne-Ardenne. The serological tests chosen will allow systematic detection of anti-SARS-CoV-2 IgM and anti-SARS-Cov-2 IgG to assess the moment of potential contamination prior to resumption of occupational activity.

Type of study:

This is a prevalence study, a single-center cross-sectional study published on the human person.

Population:

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Major volunteers from the Staff of the University of Reims Champagne-Ardenne (>18 years old)

Exclusion Criteria

  • (Non Inclusion):
  • persons who do not desire to participate

Outcomes

Primary Outcomes

Prevalence of IgG and IgM anti-SARS CoV2 antibodies

Time Frame: Inclusion time was ½ day, time for blood sampling

Anti-SARS-Cov2 seroprevalence measured in blood sample collected at Day 0.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Université de Reims Champagne-Ardenne
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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