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Clinical Trial Summary

Regional population-based registry for the epidemiological surveillance of congenital anomalies


Clinical Trial Description

By systematically collecting data on congenital anomalies, the registry aims to : - provide essential epidemiological information on congenital anomalies in South West of France - Promote etiological research concerning congenital anomalies, particularly with regard to environmental risk factors (systematic questionnaire) and other teratogenic agents (drugs) - act as an information and resource center for the population, health professionals and managers regarding clusters or exposures or risk factors of concern. - evaluate the effectiveness of primary prevention - assess the impact of developments in prenatal screening - study the fate of children with congenital anomalies, particularly in terms of neurodevelopment, through the creation of cohorts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05231447
Study type Observational [Patient Registry]
Source University Hospital, Bordeaux
Contact Julie Thomas-Chabaneix, MD
Phone (0)5 57 65 61 10
Email julie.thomas@chu-bordeaux.fr
Status Not yet recruiting
Phase
Start date March 1, 2022
Completion date March 1, 2025

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