Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06749405

Assessment of a Quantra-guided Transfusion Algorithm in Liver Transplantation

Led by University Hospital, Toulouse · Updated on 2025-09-22

56

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Liver transplantation carries a substantial risk of bleeding, making precise haemostasis control essential, although assessing coagulation remains challenging. Quantra, a bedside viscoelastic testing device using sonorheometric methods, offers an innovative approach to guiding haemostatic management during surgery. The study aims to determine whether a Quantra-guided transfusion can reduce transfusion and bleeding during liver transplantation when compared to a conventional transfusion approach.

CONDITIONS

Official Title

Assessment of a Quantra-guided Transfusion Algorithm in Liver Transplantation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • Patients with end-stage liver disease undergoing liver transplantation
  • Individuals affiliated with or beneficiaries of a social security scheme
  • Free and informed written consent obtained from the patient or a trusted person/family member/close relative
Not Eligible

You will not qualify if you...

  • Multi-organ transplantation
  • Congenital haemostasis disorders such as haemophilia
  • Patients under juridical protection (including deprived of liberty, curatorship, guardianship, or safeguard of justice)
  • Pregnant or breastfeeding women
  • Patients already enrolled in another interventional study aimed at reducing perioperative bleeding or transfusion

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Toulouse University Hospital

Toulouse, France, 31059

Actively Recruiting

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Research Team

G

Guillaume PORTA BONETE, Md

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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