Actively Recruiting
A Prospective Clinical Study of Association Between Postoperative Dyslipidemia and Organ Rejection in Heart Transplant Patients
Led by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Updated on 2023-08-16
80
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to understand how abnormal lipid metabolism, which is common after organ transplantation, relates to transplant rejection and failure. It focuses on cardiac transplant patients who often experience lipid changes due to immunotherapy. The study explores the interaction between PCSK9, lipid disorders, and immune responses, which may contribute to transplant rejection. The goal is to clarify these links to improve management of lipids during and after surgery. The study involves tracking heart transplant patients over a long term to observe lipid changes and their connection to rejection. It expands testing beyond traditional lipid assays to include transcriptomic, proteomic, and metabolomic analyses to better understand PCSK9's role in dyslipidemia. Single-cell sequencing is used to investigate how these lipid changes affect T-cell-mediated rejection of the transplanted heart. Participants will be followed for four years, during which blood lipid levels and graft/patient survival will be monitored. Additional assessments include measuring heart function through left ventricular ejection fraction at rest. This observational study collects detailed biological data and monitors health outcomes to deepen understanding of how lipid metabolism influences transplant success and patient survival.
CONDITIONS
Brief Title
A Clinical Study of Association Between Postoperative Dyslipidemia and Organ Rejection in Transplant Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- After heart transplantation
- Age 18 years or older
- Symptomatic heart failure lasting 6 months or more before screening
- Ability and willingness to provide informed consent
You will not qualify if you...
- Refusal to provide consent
- Suspected inability to follow instructions or cooperate
- Presence of another life-threatening disease with survival less than 2 years
- Participation in another clinical study within 30 days prior to screening
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 4 years
Participants who have undergone heart transplantation are observed for blood lipid levels, graft and patient survival, and heart function.
Trial Site Locations
Total: 1 location
1
Wuhan Union Hospital
Wuhan, China
Actively Recruiting
Research Team
J
Jiahong Xia
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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