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Study identifier: NCT07585890 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Establishing a Reference Framework for Outcomes After Machine-Preserved Liver Transplantation in Europe

Condition: End-stage Liver Disease (ESLD) · Acute Liver Failure · Liver Cirrhosis  ·  Sponsor: University Medical Center Groningen

PhaseN/A
Planned participants10000
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Machine perfusion (MP) has become routine clinical practice in liver transplantation. However, as the field has matured, direct randomized comparisons between distinct MP modalities have become increasingly impractical, given that donor and graft characteristics often predetermine the optimal preservation strategy. Consequently, many studies continue to reference historical benchmark cohorts from the pre-perfusion era, or use risk scores developed before routine utilization of MP. These cohorts, while once valuable, fail to account for the paradigm shift that MP has introduced. Likewise, commonly used donor- and recipient-based risk scores were developed prior to the adoption of MP. While these scores aim to assess survival or morbidity after transplantation, none of them guide decisions about MP use or the most suitable perfusion protocol. As MP technologies continue to evolve there is a critical need for an updated reference framework that accurately reflects current clinical practice and captures the best achievable outcomes across all MP modalities.

This description comes directly from the study's public registry record.

Talk to the study team

Sabrina Stimmeder, MD  ·  ‭+31503612896‬  ·  s.stimmeder@umcg.nl

Always discuss trial participation with your own doctor first.

Locations (2)

A.O.U. Città della Salute e della ScienzaTorino, ItalyRecruiting
University Medical Center GroningenGroningen, Provincie Groningen, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT07585890