Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06215404

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

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have end stage liver disease
  • Aged between 18 and 75 years old
  • Expected to receive a liver transplantation
Not Eligible

You will not qualify if you...

  • Have arrhythmia (irregular heart rhythm)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

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

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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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