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.
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