FIV-ABM - National Registry on In-Vitro Fertilization Attempts

Head :
Royère Dominique , Direction Procréation Embryologie Génétique humaine
Pessione Fabienne, Direction Procréation Embryologie Génétique humaine

Last update : 07/08/2015 | Version : 1 | ID : 8378

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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 National Registry on In-Vitro Fertilization Attempts
Sign or acronym FIV-ABM
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL approval.
General Aspects
Medical area Biology
Pathology (details) medically-assisted procreation
Health determinants Iatrogenic
Keywords IVF, MAP, registry, sterility, in-vitro fertilisation, medically-assisted procreation, infertility
Scientific investigator(s) (Contact)
Name of the director Royère
Surname Dominique
Address 1 avenue du stade de France 93212 SAINT-DENIS LA PLAINE Cedex
Phone +33 (0)1 55 93 65 50
Email dominique.royere@biomedecine.fr
Unit Direction Procréation Embryologie Génétique humaine
Organization Agence de la
Name of the director Pessione
Surname Fabienne
Address 1 avenue du stade de France 93212 SAINT-DENIS LA PLAINE Cedex
Email fabienne.pessione@biomedecine.fr
Unit Direction Procréation Embryologie Génétique humaine
Organization Agence de la
Collaborations
Funding
Funding status Public
Details Ministry of Health and Social Affairs
Governance of the database
Sponsor(s) or organisation(s) responsible Agence de la Biomédecine
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Comprehensive
Database objective
Main objective The objective of this registry is to provide a comprehensive catalogue of in vitro fertilisation activities in France (annual report on agency activity, regional analyses, etc..) and to assess the results, given associated factors such as:
- The woman (age they began smoking, indication of infertility, etc.);
- The man (smoking, indication of infertility, etc.);
- Attempt (number of attempts, gamete origin, technique used, quality of embryos, etc.);
The registry shall identify the donor couple's treatment path over several years, attempt by attempt, throughout different centres if required, and to provide recommendations in order to improve clinical practice for the patient;
To monitor pregnancy and to assess the child's health at birth through an after-birth study.
Inclusion criteria - IVF attempts (with or without ICSI) and the transfer of frozen embryos;
- Intrauterine insemination or simple ovarian stimulation is not included.
Population type
Age Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Population covered Sick population
Gender Woman
Geography area National
Detail of the geography area France
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 2008
Date of last collection (YYYY or MM/YYYY) 2012
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 50,000 per year.
Data
Database activity Current data collection
Type of data collected Clinical data
Declarative data
Biological data
Clinical data (detail) Direct physical measures
Medical registration
Details of collected clinical data patient health status, sterility assessment.
Declarative data (detail) Paper self-questionnaire
Details of collected declarative data Smoking.
Biological data (detail) Sperm analysis.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health care consumption and services
Others
Care consumption (detail) Hospitalization
Medical/paramedical consultation
Other (detail) Labour/births.
Procedures
Data collection method Computer data is exchanged between MAP clinical biology centres.
Quality procedure(s) used A data validation plan listing all quality checks for data from each progress report is established every year. This plan aims to define checks that may identify missing or inconsistent data. A data clarification request is systematically sent to centres so they may correct or clarify missing or inconsistent data.
Participant monitoring Yes
Details on monitoring of participants - Follow-up until the end of pregnancy. Child's health at birth - follow-up of MAP treatment plan for women: sequence of various attempts.
Links to administrative sources No
Promotion and access
Promotion
Access
Terms of data access (charter for data provision, format of data, availability delay) Anonymous data, statistics available on website.
Contact the scientist in charge for further information.
Access to aggregated data Free access
Access to individual data Access on specific project only

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