Last update : 05/06/2021 | Version : 1 | ID : 73902
General | |
Identification | |
Detailed name | Clinical events occurring within 6 months of SARS-COV-2 infection: multicentre cohort |
Sign or acronym | COCO_LATE |
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | CNIL MR01, favorable opinion CPP |
General Aspects | |
Medical area |
Infectious diseases Psychology and psychiatry |
Study in connection with Covid-19 |
Yes |
Scientific investigator(s) (Contact) | |
Name of the director | ROBINEAU |
Surname | Olivier |
Collaborations | |
Participation in projects, networks and consortia |
Yes |
Funding | |
Funding status |
Public |
Governance of the database | |
Sponsor(s) or organisation(s) responsible | Tourcoing Hospital |
Organisation status |
Public |
Presence of scientific or steering committees |
Yes |
Additional contact | |
Name of the contact | TREHOUX |
Surname | Solange |
recherche@ch-tourcoing.fr | |
Main features | |
Type of database | |
Type of database |
Others |
Study databases (details) |
Cohort study |
Database objective | |
Main objective |
Describe, over time, the symptoms presented by patients reporting persistent symptoms (more than two months after onset) or onset of symptoms more than 3 weeks after the beginning of symptomatic SARS-CoV-2 (COVID-19) infection evidenced by laboratory tests.
|
Inclusion criteria |
1- History of symptomatic SARS-CoV-2 infection defined by:
A positive RT-PCR result for SARS-CoV-2 OR positive SARS-CoV-2 serology combined with at least one event: - Anosmia occurring after February 2020 - OR CT scan consistent with COVID-19 - OR ? 2 symptoms coinciding with the virology sample, including: asthenia, cough, dyspnoea, fever, myalgia, dysgeusia, diarrhoea AND not present prior to diagnosis 2- AND persistence of at least one symptom present in the first 3 weeks of COVID-19, more than 8 weeks after the first COVID symptoms OR late onset of at least one new symptom at least 3 weeks and not more than 6 months after the first symptoms of SARS-CoV-2 infection 3- First symptoms within the past 6 months on the date of inclusion 4- Beneficiary of a health insurance scheme or the state welfare scheme 5- Having signed an informed consent form at inclusion |
Population type | |
Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
Population covered |
Sick population |
Pathology | B99-B99 - Other infectious diseases |
Gender |
Male Woman |
Geography area |
National |
Data collection | |
Dates | |
Date of first collection (YYYY or MM/YYYY) | 2020 |
Size of the database | |
Size of the database (number of individuals) |
[500-1000[ individuals |
Data | |
Database activity |
Current data collection |
Type of data collected |
Clinical data Paraclinical data Biological data |
Clinical data (detail) |
Direct physical measures Medical registration |
Presence of a biobank |
Yes |
Contents of biobank |
Serum Plasma |
Procedures | |
Followed pathology | |
Promotion and access | |
Promotion | |
Access |
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