Bilio-pancreatic Complications of Congenital Duodenal Obstructions
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: duodenal atresia.
- Who it may be relevant to
- Registry conditions: Duodenal Obstruction. Basic parameters: up to 16 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Congenital duodenal obstructions, often grouped under the term duodenal atresias, encompass a range of malformations of the duodenum that cause partial or complete obstruction. In the long term, the main complications described fall within the spectrum of digestive occlusions (anastomotic stenosis, obstruction due to adhesions, and duodenal dysmotility) and may require surgical revisions. Biliary and pancreatic complications, which are embryologically logical, are reported in the form of rare clinical cases. The aim of the research is to identify biliopancreatic complications following duodenal atresia surgery in order to characterize them, estimate their national frequency, and determine any potential iatrogenic risk factors.
Interventions
- Procedure duodenal atresia
surgery for duodenal atresia
Primary outcome measures
- frequency of biliar complication after surgical treatment of duodenal atresia [Time frame: 1 year]
- frequency of pancreatic complication after surgical treatment of duodenal atresia [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
- Patients who underwent surgery for duodenal atresia in a pediatric surgery department participating in the study over the past 20 years,
- legal representatives did not object to data collection
Exclusion criteria
- Patients ≥ 16 years at the time of surgery.
- Objection from the legal representatives of the child or the adult patient to the collection and use of health data
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06642805 · 49RC24_0157