← Eichor
Study identifier: NCT07301853 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Living Donor Liver Transplantation Recipients · Deceased Donor Liver Transplantation Recipients · Living Liver Donor  ·  Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University

PhaseN/A
Planned participants9999
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Wen Fang  ·  19705094680  ·  wenfang@zju.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

The Second Affiliated Hospital Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07301853