Study on the Clinical Outcomes of ABO-Incompatible Living Donor 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
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: ABO Incompatibility, Liver Transplant Surgery, Living Donor Liver Transplantation. Basic parameters: No limits · 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
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Evaluate the postoperative survival rate and incidence of rejection in patients undergoing ABO-incompatible living donor liver transplantation; analyze the occurrence of secondary endpoint events such as postoperative vascular complications and biliary complications; and explore relevant risk factors affecting prognosis.
Detailed description
Prospective and retrospective
Primary outcome measures
- Postoperative survival rate [Time frame: Minimum follow-up period of 1 year postoperatively.]
- incidence of acute rejection [Time frame: Within 1 year postoperatively]
Secondary outcome measures (2)
- Vascular complications [Time frame: Within 1 year postoperatively]
- Biliary complications [Time frame: Within 1 year postoperatively]
Eligibility criteria
Inclusion criteria
- Underwent ABO-incompatible living donor liver transplantation
- Complete and intact clinical and follow-up data
Exclusion criteria
- Non-primary liver transplantation
- Combined other organ transplantation
- Incomplete clinical data or loss to follow-up
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
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07273448 · BFH20251127006