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