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Clinical Trials in South Korea / NCT06767553
Active, not recruiting Observational

Biliary Complication Rates in Living Donor Liver Transplantation: a Retrospective Comparative Study of Stent Versus Non-Stent Groups

NCT06767553 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2011-11-01
Last updated
2025-01-10

Condition(s) studied

Liver FailureLiving Donor Liver TransplantationBiliary ComplicationsBiliary Stents

Study summary

Despite technological advancements in living donor liver transplantation (LDLT), biliary complications (BC), including biliary anastomotic stricture (BAS) and bile leak (BL), remain unresolved issues that significantly affect patient outcomes. Biliary stenting has emerged as a potential method for reducing BC in LDLT procedures; however, their necessity remains debated. This study aimed to assess the necessity of biliary stenting by retrospectively comparing the bile duct complication rates in LDLT using duct-to-duct anastomosis with or without biliary stenting.

Eligibility

Sex
ALL
Min age
19 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged between 19 and 80 years at the time of liver transplantation. * Patients who underwent liver transplantation surgery for liver disease performed by the Department of Surgery at Chungnam National University Hospital under the supervision of the principal investigator. * Patients who signed the informed consent form before study registration (for future participants). Exclusion Criteria: * Patients who have not signed the informed consent form or have insufficient understanding of the clinical trial protocol, making it difficult to accurately express their intention to participate. * Patients deemed unsuitable for participation in this clinical study by the investigator.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chungnam National University Hospital Daejeon South Korea

More Chungnam National University Hospital trials in South Korea

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06767553 on ClinicalTrials.gov ↗ ← All trials in South Korea