Recruiting NCT05761483
Endoscopic Management of Non-anastomotic Biliary Strictures Following Liver Transplantation.
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 →
Unsure about the terms? Read our patient guide →
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