Actively Recruiting
Longitudinal Follow-up and Health-Related Outcomes in Liver Transplant Recipients and Living Donors
Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2025-12-24
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Participants Needed
1
Research Sites
1048 weeks
Total Duration
On this page
Sponsors
S
Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead Sponsor
M
Mukogawa Women's University
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Longitudinal Follow-up and Health-Related Outcomes in Liver Transplant Recipients and Living Donors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Second Affiliated Hospital Zhejiang University School of Medicine
Hangzhou, Zhejiang, China, 310009
Actively Recruiting
Research Team
W
Wen Fang
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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