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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04481529
Other study ID # 87RI20_0049/SEROCO
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 29, 2020
Est. completion date January 15, 2021

Study information

Verified date November 2020
Source University Hospital, Limoges
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hospital staff, on the front line in the COVID-19 crisis, have many questions about the risk that they have been infected with this potentially fatal virus. These questions of course primarily concern caregivers working in sectors dedicated to COVID-19 patients, whether they are resuscitating or not, but also those in non-COVID-19 sectors, or even staff without direct contact with patients. In addition, depending on the suddenness and intensity of this "COVID-19 wave", these personnel have been more or less trained and sometimes exposed due to the dire lack of protective equipment. In some countries such as Great Britain, this has resulted in significant absenteeism, a source of deepening the shortage of caregivers. This proportion of contaminated caregivers has not been evaluated on the whole of French territory. Studies from other countries suggest figures ranging from 1.5% in China to 20% in Italy. It is therefore impossible to rely on such variable data to have a reliable estimate. Since june 2020, all staff in French health establishments could benefit a serological test. Thus, in this epidemiological study, we propose to rely on this institutional serological screening to describe the link between seroconversion of hospital staff, regional intensity of the epidemic, and sectors of activity (COVID-19 sectors, non-COVID-19 caregivers , non-COVID-19 non-caregivers.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1576
Est. completion date January 15, 2021
Est. primary completion date December 15, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hospital staff from Argenteuil, Belfort, Dijon and Limoges hospitals. - Age = 18 years old - Participation agreement Exclusion Criteria: - Protected persons - Refusal of participation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Health Questionnaire
Completion of a short questionnaire noting the result of the serology and looking for elements in favor of exposure to the virus, whether professional or extra-professional.

Locations

Country Name City State
France CH Argenteuil - Service de Réanimation Argenteuil
France Ch Belfort Belfort
France CHU Dijon - Serve de Réanimation Dijon
France CHU de Limoges Limoges

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Limoges

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of subjects with a COVID-19 seroconversion Number of subjects with a COVID-19 seroconversion fixed by the presence of IgG + in serology according to the service (COVID19 +, COVID19- caregiver, COVID- non-caregiver). through study completion, an average of 5 month
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