Bilio-pancreatic Complications of Congenital Duodenal Obstructions

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

450 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-31

Study Completion Date

2025-12-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Duodenal Obstruction

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Cohort bilious

duodenal atresia

Intervention Type PROCEDURE

surgery for duodenal atresia

Interventions

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duodenal atresia

surgery for duodenal atresia

Intervention Type PROCEDURE

Eligibility Criteria

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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

Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No