- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04371692
Prevalence of COVID-19 Infection Among HCW in a French University Hospital (EXPOCOVIA)
April 22, 2021 updated by: University Hospital, Lille
Prevalence of SARS-Cov2 Infection Among HCW in Lille University Hospital
The objective of this study is to determine the prevalence of SARS-Cov2 infection among health care workers exposed of Lille University Hospital, to describe its evolution during the epidemic taking into account the influence of occupational and environmental exposure determinants.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
900
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Lille, France, 59037
- Hop Claude Huriez Chu Lille
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Health Care workers with or without symptoms suggestive of a COVID-19 infection
Description
Inclusion Criteria:
- Health Care workers with or without symptoms suggestive of a COVID-19 infection
Exclusion Criteria:
- HCW working off-site at the CHU de Lille
- HCW on sick leave.
- HCW outside the Lille University Hospital temporarily coming as reinforcements in the context of the epidemic.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
High-risk
staff working in a unit specifically for patients infected or suspected of being infected with SARS-Cov2
|
Every weeks during 2 months, clinical and occupational questionnaire are performed among a cohort of HCW exposed to covid occupational exposure
Other Names:
Every weeks during 2 month, SARS-Cov2 RT-PCR, serological testing are performed among a cohort of HCW exposed to covid occupational exposure
|
Medium- risk
staff working in a unit that can accommodate patients infected or suspected of being infected with SARS-Cov2, i.e., all care services that do not fall into the high-risk group.
|
Every weeks during 2 months, clinical and occupational questionnaire are performed among a cohort of HCW exposed to covid occupational exposure
Other Names:
Every weeks during 2 month, SARS-Cov2 RT-PCR, serological testing are performed among a cohort of HCW exposed to covid occupational exposure
|
Low-risk
off-patient staff
|
Every weeks during 2 months, clinical and occupational questionnaire are performed among a cohort of HCW exposed to covid occupational exposure
Other Names:
Every weeks during 2 month, SARS-Cov2 RT-PCR, serological testing are performed among a cohort of HCW exposed to covid occupational exposure
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the prevalence of SARS- Cov2 infection Health Care Worker with or without symptoms suggestive of a COVID-19 infection
Time Frame: at 2 months
|
at 2 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the prevalence of SARS- Cov2 infection Health Care Worker with or without symptoms suggestive of a COVID-19 infection
Time Frame: once week during 2 months
|
once week during 2 months
|
Occupational exposures associated with the SARS-Cov2 infection
Time Frame: once week during 2 months
|
once week during 2 months
|
Environmental exposures associated with the SARS-Cov2 infection
Time Frame: once week during 2 months
|
once week during 2 months
|
immunologic status of health Care Worker
Time Frame: once week during 2 months
|
once week during 2 months
|
inflammatory biomarkers status of Health Care Worker
Time Frame: once week during 2 months
|
once week during 2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Annie SOBASZEK, MD, University Hospital, Lille
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 15, 2020
Primary Completion (Actual)
July 9, 2020
Study Completion (Actual)
July 9, 2020
Study Registration Dates
First Submitted
April 28, 2020
First Submitted That Met QC Criteria
April 28, 2020
First Posted (Actual)
May 1, 2020
Study Record Updates
Last Update Posted (Actual)
April 23, 2021
Last Update Submitted That Met QC Criteria
April 22, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020_35
- 2020-A00951-38 (Other Identifier: ID-RCB number,ANSM)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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