Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Previous endoscopic or percutaneous treatments
- Candidate for metal stent placement
- Previous surgery causing altered anatomy
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Not specified
Participants undergo diagnostic procedures such as Endoscopic Retrograde Cholangiopancreatography (ERCP) to assess biliary strictures.
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
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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