COroFET - Clinical and laboratory epidemiological monitoring of pregnant women with evaluation of the obstetric, foetal and neonatal risk associated with SARS-CoV-2 during the COVID-19 pandemic– COroFET 

Head :
DUBUCS Charlotte, IUCT-Oncopole Pathology Department

Last update : 05/05/2021 | Version : 1 | ID : 73499

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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
Promotion
Access
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General
Identification
Detailed name Clinical and laboratory epidemiological monitoring of pregnant women with evaluation of the obstetric, foetal and neonatal risk associated with SARS-CoV-2 during the COVID-19 pandemic– COroFET 
Sign or acronym COroFET
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CPP2020-04-039 / 2020-A00870-39 / 20.04.07.83722
General Aspects
Medical area Anatomy - Cytology
Gynecology/ obstetrics
Infectious diseases
Study in connection with Covid-19 Yes
Scientific investigator(s) (Contact)
Name of the director DUBUCS
Surname Charlotte
Address 1 avenue Irène Joliot-Curie<br>31100 TOULOUSE
Phone 531156193
Email dubucs.charlotte@iuct-oncopole.fr
Unit IUCT-Oncopole Pathology Department
Organization Toulouse University Hospital
Collaborations
Funding
Governance of the database
Sponsor(s) or organisation(s) responsible Toulouse University Hospital
Organisation status Public
Additional contact
Main features
Type of database
Type of database Others
Specify Clinical and laboratory database (containing clinical and paraclinical data associated with a biological and tissue collection on pregnancy outcomes)
Database recruitment is carried out as part of an interventional study No
Database objective
Main objective In this situation in which data are crucial to understanding the effects of SARS-CoV-2 in the pregnant female population, our primary objective is to collect clinical and paraclinical data from a large sample of women recruited from our level 3 maternity unit, and to create biological and tissue collections with a view to responding to a series of questions, partly explained in the research programme, but which may also evolve as knowledge progresses.
Inclusion criteria Adult females aged 18 years or over at the date of inclusion
Pregnant women giving birth at the Paule de Viguier maternity unit, Toulouse University Hospital, in the study, between April 2020 and April 2021, regardless of pregnancy outcome (live births, intrauterine foetal death, termination of pregnancy, i.e. miscarriages, medical termination of pregnancy) and term
Women having given their consent to take part in the study
Women registered with a social security scheme (including the state welfare scheme)
Population type
Age Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Population covered General population
Pathology
Gender Woman
Geography area Regional
French regions covered by the database Languedoc-Roussillon Midi-Pyrénées
Detail of the geography area Toulouse
Data collection
Dates
Size of the database
Size of the database (number of individuals) [1000-10 000[ individuals
Details of the number of individuals target 3,600 by end April 2021
Data
Database activity Current data collection
Type of data collected Clinical data
Paraclinical data
Biological data
Clinical data (detail) Direct physical measures
Presence of a biobank Yes
Contents of biobank Serum
Cord blood
Fluids (saliva, urine, amniotic fluid, …)
Tissues
Procedures
Participant monitoring No
Followed pathology
Links to administrative sources No
Promotion and access
Promotion
Access

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