Skip to content

Laparascopic vs. Laparotomy Management of Neonatal Duodenal Atresia

Laparascopic vs. Laparotomy Management of Neonatal Duodenal Atresia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06115226
Enrollment
70
Registered
2023-11-02
Start date
2020-03-13
Completion date
2023-12-31
Last updated
2023-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Duodenal Atresia

Keywords

Congenital duodenal atresia, Neonatal obstruction, Laparascopic, Laparotomy, Neonatal duodenal atresia

Brief summary

Congenital duodenal atresia is a common cause of neonatal obstruction affecting 1 in 5000-10000 neonates. Laparoscopic management of this malformation is becoming increasingly common. However, few comparative studies exist and are often monocentric including few patients. This study will be multicentric, international and comparative to determine the place of laparoscopic surgery in the management of congenital duodenal atresia.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 17 Years
Healthy volunteers
No

Inclusion criteria

* Minor subject * Subject having undergone neonatal surgery for congenital duodenal atresia or stenosis in the different participating centers between January 2009 and December 2019 * Subject (and/or his/her parental authority) who has not expressed, after information, his/her opposition to the reuse of his/her data for the purpose of this research Criteria for non-inclusion: * Subject (and/or his/her parental authority) who has indicated, after information, his/her opposition to the re-use of his/her data for the purposes of this research * Conversion linked to a renunciation of the surgeon, procedure not started (optical introduction, unfeasibility by the surgeon due to lack of experience or technical impossibility)

Design outcomes

Primary

MeasureTime frame
rate of complications3 months after laparoscopic surgery

Countries

France

Contacts

Primary ContactFrançois BECMEUR, MD, PhD
francois.Becmeur@chru-strasbourg.fr33.3.88.12.73.07

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026