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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05616663
Other study ID # 7954
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 31, 2020
Est. completion date December 16, 2023

Study information

Verified date December 2023
Source University Hospital, Strasbourg, France
Contact Maria GONZALEZ, MD, PhD
Phone 33 3 88 11 64 66
Email maria.gonzalez@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Started on January 9, 2020 with the announcement of the discovery of a new SARS-CoV-2 coronavirus, the Covid-19 pandemic is responsible as of June 21, 2020 for 160,377 confirmed cases in France, 29,640 deaths and 9,823 hospitalizations. The Grand Est region is one of the regions in France that was most precociously and strongly affected by the epidemic, in particular the Strasbourg University Hospital. Faced with the heavy use of the healthcare system, hospital staff of all categories are an essential resource to be preserved. Several studies have shown the significant impact of Covid-19 on doctors and caregivers. In order to better protect these personnel and avoid contamination that could be harmful to their health but also because of the consequences in terms of staff, it is necessary to better understand the risk factors for transmission of this infection, the means of protection, the evolution of the disease and the determinants of the return to work. Few studies have explored on such a large workforce and in detail the professional risk factors for developing Covid-19 within different groups of hospital professionals including also non-caregivers and the evolution when returning to work in an outpatient population.


Recruitment information / eligibility

Status Recruiting
Enrollment 639
Est. completion date December 16, 2023
Est. primary completion date December 16, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Major subject (=18 years old) - Professionals from the University Hospitals of Strasbourg (HUS) - Professionals who had been working at the HUS at the time of the diagnosis of SARS CoV-2 infection. - Subject having not expressed, after being informed, opposition to the reuse of their data for research purposes Exclusion criteria: - Subject who expressed their opposition to participating in the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de Pathologie Professionnelle et Médecine du Travail - CHU de Strasbourg - France Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary positive RT-PCR test The presence of SARS CoV 2 infection is assessed by a positive RT-PCR test one week after infection with Covid-19
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