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OpenTrials
Completed

NCT Number: NCT01447030

Long Time Follow up After HJ Following Iatrogenic Bile Duct Injuries

Introduction: Bile duct injury (BDI) after cholecystectomy remains a serious complication with major implications for patient outcome. For most major BDIs, the recommended method of repair is a hepaticojejunostomy (HJ). We conducted a retrospective review from 5 Danish hepatobiliary centres aiming to examine the perioperative and the long-term outcome after reconstructive HJ.

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Key information

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients with iatrogenic Bile duct injury (BDI) after cholecystectomy reconstructed with hepatojejunostomy/choledochojejunostomy.

Exclusion criteria

  • Patients with non-cholecystectomy-related BDI or with cholecystectomy-related BDI that had been definitively managed by other techniques.

Treatment and study plan

Primary outcomes

  1. Stricture of HJ

    Time frame: days to years

    Stricture of hepaticojejunostomy after reconstruction

Sponsors and collaborators

Lead sponsor

Odense University Hospital

Other

Collaborators

  • Aalborg University Hospital
  • Aarhus University Hospital
  • Herlev Hospital
  • Rigshospitalet, Denmark

Registry information

Official study title

Langtidsopfølgning Efter Kirurgisk Behandling af Iatrogene galdevejslæsioner opstået i Forbindelse Med Cholecystektomi

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Oct 5, 2011
Registry last updated
Mar 9, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.