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Recruiting NCT05761483

Endoscopic Management of Non-anastomotic Biliary Strictures Following Liver Transplantation.

Observational Liver Transplant Disorder Ischemic Cholangiopathy Non-anastomotic Biliary Stricture Biliary Stricture

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: ERCP.
Who it may be relevant to
Registry conditions: Liver Transplant Disorder, Ischemic Cholangiopathy, Non-anastomotic Biliary Stricture, Biliary Stricture. Basic parameters: from 18 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
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Endoscopic Management of Non-anastomotic Biliary Strictures Following Liver Transplantation. Registry of the Italian Society of Digestive Endoscopy.

Overview

The study will evaluate the results of endoscopic treatment of NON-anastomotic biliary strictures following liver transplantation

Interventions

  • Procedure ERCP
    Endoscopic Retrograde Cholangiopancreatography, placement of stents using a duodenoscope and making an access through the papilla of Vater

Primary outcome measures

  • Evaluation of endoscopic treatment of non-anastomosis biliary strictures [Time frame: 2 Years follow-up]

Eligibility criteria

Inclusion criteria

  • Age > 18
  • Non anastomotic biliary strictures diagnosed by direct cholangiogram (T-tube) or MRCP
  • Stricture involving the hepatic hilum until secondary branches
  • Increase of liver function tests
  • Signature of the informed consent

Exclusion criteria

  • Previopus endoscopic or percutaneous treatments
  • Patient candidate to metal stents placement
  • Previous surgery resulting in altered anatomy

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

Italy · 1 center
  • Fondazione Policlinico Gemelli IRCCS — Roma

Identifiers

NCT: NCT05761483 · 2766

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗