FRANCE | WP5 | |||
Organization | INSERM-APHP | |||
Name of cohort | CoV-CONTACT | |||
Referring partner | AP-HP | |||
Cohort Information | Country(-ies), cities, regions or centers involved | France | ||
Time of data collection | 03/2020 | 01/2023 | ||
Enrolment | Inactive | |||
Study setting | Multi-centers | |||
Population | Age | Adults | ||
Type | Prospective | |||
Total number of patients | 317 | |||
Data collection | Clinical data | True | ||
Serological data | True | |||
Genetic data | False | |||
Sample collection | True | |||
Sample collected | Whole blood | Yes | ||
PBMC | No | |||
Dry-spot blood | No | |||
Plasma | No | |||
Serum | No | |||
Stool | No | |||
NP swabs | Yes | |||
Other | None | |||
Description | Cov-CONTACT is a prospective cohort in HCWs who had a high-risk exposure to SARS-CoV-2-infected subject without personal protective equipment. Daily symptoms are self-reported for 30 days, nasopharyngeal swabs for SARS-CoV-2 RT-PCR are performed at inclusion and at days 3, 5, 7 and 12, SARS-CoV-2 serology is assessed at inclusion and at day 30. Confirmed infection is defined by positive RT-PCR or seroconversion, and possible infection by one general and one specific symptom for two consecutive days. |