Portal Inflow Modulation Prior to Liver Transplantation in Patients With Increased Risk of Intraoperative Blood Loss

Recruiting N/A Interventional Study
Liver Cirrhosis Clinically Significant Portal Hypertension
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
104 (estimated)
Sponsor
Medical University of Warsaw · Other
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About This Trial
Liver transplantation is a procedure associated with an exceptionally high risk of blood loss. Liver failure, which is the most common indication for transplantation, not only leads to coagulation disorders but also to the development of portal hypertension. As a result, collateral circulation forms within the abdominal venous system, significantly increasing the risk of massive intraoperative blo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Qualification for elective liver transplantation from a deceased donor * Age ≥18 years * BMI between 18.5 kg/m² and 30 kg/m² * Informed consent to participate in the study * Clinically significant portal hypertension * At least 1 of the following risk factors for massive blood…
Contacts

Wacław Hołówko, dr hab. n. med.

+48 667 667 044

waclaw.holowko@wum.edu.pl

CONTACT

Zuzanna Łuczak

luczakpresite@gmail.com

CONTACT