The goal of this study is to find out if quality assessment by normothermic machine perfusion can be used to safely increase the number of usable donor livers, helping more people get transplants faster and with better results. This process keeps a donated liver working outside the body before transplantation, allowing surgeons to assess whether livers previously considered unsuitable can still be used. The main questions this study aims to answer are: * Does this method help patients get a transplant sooner? * Can this method make more livers available for transplant? * Does it improve survival and health after transplant? Participants in this study must be on the waiting list for a liver transplant with a ReMELD-Na-Score of 21 or less (equivalent to MELD ≤25) and must not qualify for certain special exceptions. Participants will be randomly placed into one of two groups: * Experimental group: In addition to regular organ offers, these participants may receive a liver that was initially not considered for transplantation but meets quality standards after at least four hours of machine perfusion. * Control group: These participants will receive a liver through the usual transplant process. The main measure of success is how quickly participants receive a transplant. Researchers will also look at other important factors, such as survival rates, quality of life, hospital stay, and complications after transplant. This study may help improve liver transplantation by making better use of available donor livers, reducing waiting times, and improving patient outcomes.
Liver transplantation is the treatment of choice for patients with advanced liver cirrhosis, hepatocellular carcinoma within the Milan criteria, and severe metabolic or autoimmune liver diseases. However, organ shortage remains a significant issue, particularly in Germany, where only 58% of patients on the waiting list received a transplant in 2022. Patients with MELD ≤25, who are ineligible for \[Non\]-Standard Exception criteria, face particularly long waiting times and lower transplant rates. Despite the shortage, approximately 24% of all liver grafts in Germany are declined due to donor age, macrosteatosis, or prolonged cold ischemia. Emerging technologies, such as NMP, allow for objective graft quality assessment before transplantation. Several non-randomized studies in the UK, Netherlands, Australia, and the USA have demonstrated the potential of NMP to increase organ utilization. The ExTra trial is the first randomized controlled study to investigate whether declined liver grafts, following NMP-based quality assessment, can safely and effectively reduce the waiting time for patients with ReMELD-Na-Score ≤ 21(equivalent to MELD ≤25).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
186
Quality assessment using NMP in the experimental arm is performed according to previously published viability criteria for initially declined liver grafts, which are mandatory for all participating study centers, with minor device-specific modifications. These criteria are based on the Birmingham criteria used in the VITTAL trial for viability assessment of DBD and DCD grafts with the OrganOx Metra device and are comparable to the Groningen criteria used with the LiverAssist and PerLife device, with the exception of biliary viability. These criteria are: Lactate clearance \< 2.5 mmol/L, And two or more of the following: Evidence of bile production, maintenance of a perfusate pH \>7.30 (without correction for at least one hour), glucose metabolism (falling perfusate glucose value with consistent downward trend), maintenance of stable arterial and portal venous flows (OrganOx Metra: 150 and 500 mL/min respectively), homogeneous perfusion with soft consistency of the parenchyma.
University Medical Center Hamburg-Eppendorf
Hamburg, Hamburg, Germany
RECRUITINGUniversity Hospital RWTH Aachen
Aachen, North Rhine-Westphalia, Germany
RECRUITINGUniversity Hospital Bonn
Bonn, North Rhine-Westphalia, Germany
RECRUITINGUniversity Hospital Muenster
Münster, North Rhine-Westphalia, Germany
RECRUITINGDepartment of Surgery Campus Charité Mitte | Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin
Berlin, State of Berlin, Germany
RECRUITINGDepartment of General, Visceral and Transplantation Surgery, LMU University Hospital, LMU Munich
München, Germany
RECRUITINGDepartment of Surgery, University Hospital Regensburg
Regensburg, Germany
RECRUITINGEberhard Karls University of Tübingen, Department of General Visceral and Transplant Surgery
Tübingen, Germany
RECRUITINGDepartment of General, Visceral, Transplantation, Vascular, and Pediatric Surgery, University Hospital Wurzburg
Würzburg, Germany
RECRUITINGTime-to-Transplant
Time frame: From date of randomization to liver transplantation (up to 12 months after date of randomization)
Death
Patient death during the 12-month intervention period, regardless of liver transplantation or not.
Time frame: From date of randomization to death (up to 12 months after date of randomization)
Disease Progression
Change of ReMELD-Na-Score above 21 while listed as "transplantable" on the waitlist. Occurence of new contraindication for liver transplantation
Time frame: From date of randomization to event (up to 12 months after date of randomization)
Proportion of Patients Recovered on the Waitlist
Proportion of patients with change in overall health that no liver transplantation is further required in relation to all patients on the waitlist in the trial.
Time frame: From date of randomization to event (up to 12 months after date of randomization)
Number of patients listed for transplantation after 12 months
Number of patients listed for transplantation after 12 months.
Time frame: 12 months after randomization
Overall patient survival
Overall patient survival in the study.
Time frame: From date of randomization to death (up to 24 months after date of randomization)
Patient-reported Quality of Life
Patient-reported Quality of Life measured in the EuroQOL EQ5DL. Two aspects will be reported: The EuroQOL visual analog scale (EQ VAS) on a scale from 0-100 points and the proportion of responses by level of severity for the five EQ-5D-5L dimensions (each reported on a five level scale).
Time frame: up to 24 months
Graft utilization rate
Proportion of used livers of all organs offered to patients on the waiting list
Time frame: up to 12 months
Inpatient Costs for Liver Transplantation
Analysis of liver transplantation-associated costs. This will be total costs, earnings and profit measured in Euros (EUR) for the primary inpatient stay of liver transplantation.
Time frame: First 90 days after liver transplantation
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