Actively Recruiting

Age: 18Years +
All Genders
ID05761483

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

Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2026-01-29

40

Participants Needed

1

Research Sites

61 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the results of endoscopic treatment for non-anastomotic biliary strictures that occur after liver transplantation. These strictures affect the bile ducts and can impact liver function, with the study focusing on patients diagnosed by imaging methods such as direct cholangiogram or MRCP. The study is observational and sponsored by Fondazione Policlinico Universitario Agostino Gemelli IRCCS. Participants undergo a procedure called Endoscopic Retrograde Cholangiopancreatography (ERCP), which involves using a duodenoscope to place stents through the papilla of Vater to treat the biliary strictures. The focus is on strictures located from the hepatic hilum to secondary branches. No experimental drugs are involved as this is an observational registry study. During the study, researchers will follow participants for up to two years to assess the effectiveness of the endoscopic treatment. Evaluations include monitoring liver function tests and imaging to observe changes in biliary strictures. Participants provide informed consent and receive standard clinical care, with data collected to help improve understanding of treatment outcomes for biliary strictures after liver transplantation.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18
  • Diagnosis of non-anastomotic biliary strictures by direct cholangiogram (T-tube) or MRCP
  • Stricture involving the hepatic hilum up to secondary branches
  • Increased liver function tests
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Previous endoscopic or percutaneous treatments
  • Candidate for metal stent placement
  • Previous surgery causing altered anatomy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Not specified

Participants undergo diagnostic procedures such as Endoscopic Retrograde Cholangiopancreatography (ERCP) to assess biliary strictures.

Long-term Monitoring

Duration - Up to 2 years

Participants are monitored for up to 2 years to evaluate the outcomes of endoscopic treatment for non-anastomotic biliary strictures.

Trial Site Locations

Total: 1 location

1

Fondazione Policlinico Gemelli IRCCS

Roma, RM, Italy, 00168

Actively Recruiting

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Research Team

A

Andrea Tringali, MD, PD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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