Clinical Trial: National Register of Oesophageal Atresia
Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Observational
Official Title: National Register of Oesophageal Atresia
Brief Summary:
The esophageal atresia is a group of birth defects including a break in continuity of the esophagus with or without persistent communication with the trachea (tracheoesophageal fistula), sometimes associated (from 50%) of other malformations (heart, kidney, digestive ...).
The current prognosis for this ailment is good. However he persists a mortality (<10%) and significant morbidity, firstly related malformations (heart, kidney, for example), and secondly with particularly difficult anatomical forms (Forms long defect) .
The prevalence of this condition is estimated to be 1/2500 in 3000 live births, making an estimated ± 2,500 new cases over to 10 years in France.
The current project aims to set up a national registry (Metropolitan France and Dom Tom) to measure the prevalence of esophageal atresia among live births, phenotypic characteristics, the circumstances of their diagnosis, and their initial future at short-term during the first year of life, at which time occurs the vast majority of deaths and complications in this disease.
Detailed Summary:
Sponsor: University Hospital, Lille
Current Primary Outcome: Number of esophageal atresia [ Time Frame: 10 years ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- Data collection patient with esophageal atresia [ Time Frame: 10 years ]Circumstances of diagnosis, modalities of follow-up and clinical management
- Total number of patients with complications [ Time Frame: 10 years ]
- Death [ Time Frame: 10 years ]
Original Secondary Outcome: Same as current
Information By: University Hospital, Lille
Dates:
Date Received: August 18, 2016
Date Started: November 2008
Date Completion: November 2018
Last Updated: September 21, 2016
Last Verified: September 2016
