RecruitingNot Applicable

Longitudinal Follow-up and Health-Related Outcomes in Liver Transplant Recipients and Living Donors

China9,999 participantsStarted 2025-11-24

Plain-language summary

This prospective cohort study aims to identify risk factors for postoperative adverse events in liver transplant recipients and living donors. By collecting comprehensive clinical data and conducting systematic long-term follow-up, the researchers intend to establish a specialized, standardized, and individualized follow-up management system. The ultimate goal is to optimize intervention strategies and improve patient prognosis and quality of life for both recipients and donors.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Patients undergoing liver transplantation or living donor hepatectomy at the study center (living donor should be approved by the hospital ethics committee for living organ donation);
✓. Age 18 years or older;
✓. Willing to participate in the long-term follow-up management program;
✓. Signed informed consent form;

Exclusion criteria

✕. Patients undergoing combined organ transplantation
✕. Patients with severe mental illness or cognitive impairment who are unable to cooperate with follow-up assessments.
✕. Donors whose surgery is aborted intraoperatively for any reason.
✕. Unable or unwilling to comply with the long-term follow-up schedule.

What they're measuring

Long-term Incidence of Postoperative Adverse Events

Timeframe: From date of surgery up to 20 years

Trial details

NCT IDNCT07301853

SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2045-12-31

Contact for this trial

Wen Fang

19705094680 wenfang@zju.edu.cn

View on ClinicalTrials.gov More Living Donor Liver Transplantation Recipients trials