Actively Recruiting
Effects of Different Fluid Management Strategies on Blood Loss, Inflammatory Response, and Major Organ Sequelae in Liver Transplantation
Led by National Taiwan University Hospital · Updated on 2025-04-11
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating different fluid management strategies during liver transplantation to reduce bleeding and improve patient outcomes. Due to the complexity of liver transplant surgery and issues with abnormal blood clotting, patients often experience significant bleeding requiring blood transfusions. Excessive transfusion can lead to lung complications and affect recovery. This study aims to compare restrictive and liberal fluid infusion approaches and their effects on bleeding, inflammation, and organ function after surgery. The trial randomly assigns participants to one of two groups. The liberal group receives fluid management targeting a stroke volume variation (SVV) of less than 10%, while the restrictive group targets an SVV of less than 18%. The PiCCO cardiopulmonary volume monitor is used to guide fluid administration during surgery. Researchers will observe the impact of these strategies on blood loss and organ function, including the lungs and kidneys. Participants will be closely monitored throughout the liver transplant operation and up to postoperative day 1. Measurements include blood loss during surgery, inflammatory responses, and biomarkers indicating lung and kidney injury. The study also tracks clinical care and any postoperative complications affecting major organs. This approach aims to identify the most appropriate fluid management method to support recovery after liver transplantation.
CONDITIONS
Brief Title
Fluid Management Strategies on Blood Loss in Liver Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Have end stage liver disease
- Aged between 18 and 75 years old
- Expected to receive a liver transplantation
You will not qualify if you...
- Have arrhythmia (irregular heart rhythm)
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 - Duration of the surgery and immediate recovery period
Participants undergo liver transplantation surgery during which different fluid management strategies are applied to manage blood loss and inflammatory responses.
1 surgery visit (in-person)
Trial Site Locations
Total: 1 location
1
National Taiwan University Hospital
Taipei, Taiwan
Actively Recruiting
Research Team
K
Kuang-Cheng Chan, M.D.,PhD.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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