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Study identifier: NCT02784119 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

APCext : Effect of Temporary Porto-caval Shunt During Liver Transplantation on Function of Liver Graft From Extended Criteria Donor

Condition: Liver Transplantation  ·  Sponsor: Rennes University Hospital

PhaseNA
Planned participants214
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The success of orthotopic liver transplantation (OLT) in treatment of liver malignancy and endstage liver disease has led to an increase in the gap between patients on waiting-lists and available liver grafts. In order to compensate for this scarcity, use of liver grafts harvested from extended criteria donors (ECD) has become more and more frequent. However, these ECD grafts are known to be associated with a higher rate of primary non function (PNF) or early allograft dysfunction (EAD) because of a greater vulnerability to ischemia-reperfusion injury (IRI). During OLT, the clamping of the portal vein induces blood congestion in the splanchnic territory leading to increased gut permeability, bacterial translocation and release of endotoxin and pro-inflammatory cytokines at revascularisation, which exacerbate IRI. Realisation of a temporary porto-caval shunt (TPCS) (i.e. end to side anastomosis between the portal vein and infrahepatic vena cava) during the anhepatic phase, avoids splanchnic congestion and could therefore decrease IRI and improve liver graft function. However, TPCS remains poorly used as no randomised trial succeeds to show its benefit on liver function due to lack of power.

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

Talk to the study team

Michel RAYAR, MD, PhD  ·  02 99 28 42 65  ·  michel.rayar@chu-rennes.fr

Anne GANIVET  ·  02 99 28 25 55  ·  anne.ganivet@chu-rennes.fr

Always discuss trial participation with your own doctor first.

Locations (6)

CHU BordeauxBordeaux, FranceRecruiting
Hospices Civils LyonLyon, FranceRecruiting
CHU NiceNice, FranceRecruiting
CHU RennesRennes, FranceRecruiting
CHU ToulouseToulouse, FranceRecruiting
CHU ToursTours, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT02784119