跳至主要内容
临床试验/NCT07692490
NCT07692490招募中不适用

Avoiding Recooling After Normothermic Machine Perfusion in Liver Transplantation: a Multicenter, Parallel-group, Open-label, Non-inferiority Randomized Controlled Trial

The Mediterranean Institute for Transplantation and Advanced Specialized Therapies14 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2026年7月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
170
试验地点
14
主要终点
Early Allograft Dysfunction (EAD)

研究概览

简要总结

The ARANMP-LT study is a multicenter, open-label, randomized, parallel-group, non-inferiority clinical trial designed to evaluate whether avoiding graft recooling after normothermic machine perfusion (NMP) improves early outcomes following liver transplantation. Although graft recooling before implantation is common practice, experimental and preliminary clinical evidence suggests that abrupt temperature changes may contribute to ischemia-reperfusion injury.

Adult recipients of deceased-donor liver grafts preserved with NMP or sequential hypothermic-normothermic machine perfusion (SHNMP) will be randomized in a 1:1 ratio to either standard graft implantation with recooling using cold preservation solution (control group) or implantation without recooling using a room-temperature 5% albumin flush immediately before reperfusion (intervention group).

The primary objective is to compare the incidence of Early Allograft Dysfunction (EAD), defined according to the Olthoff criteria, between the two treatment groups. Secondary objectives include evaluation of histopathological ischemia-reperfusion injury using the Suzuki score, vascular and biliary complications, primary non-function, post-reperfusion syndrome, patient and graft survival, length of intensive care unit and hospital stay, perioperative transfusion requirements, and safety outcomes. A total of 170 participants will be enrolled across multiple Italian liver transplant centers and followed for 90 days after transplantation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥18 years.
  • Listed for primary liver transplantation at the participating institution.
  • Assigned a liver graft preserved with normothermic machine perfusion or sequential hypothermic- normothermic machine perfusion (SHNMP).
  • Signed and dated informed consent prior study inclusion.

排除标准

  • Pediatric patients (age < 18 years)
  • Patients undergoing re-transplantation (history of previous liver transplantation)
  • Patients with acute liver failure
  • Patients undergoing multi-organ transplantation (e.g., liver-kidney, liver-heart)
  • Temporarily unconscious patients
  • Patients unable to freely express consent.

研究组 & 干预措施

No Recooling

Experimental

No Recooling Before Liver Implantation

干预措施: No Recooling Before Liver Implantation (Procedure)

Traditional Recooling

Active Comparator

Traditional Recooling Before Liver Implantation

干预措施: Traditional Recooling Before Liver Implantation (Procedure)

结局指标

主要结局

Early Allograft Dysfunction (EAD)

时间窗: Within 7 days after liver transplantation

Incidence of Early Allograft Dysfunction (EAD), defined according to the Olthoff criteria as bilirubin ≥10 mg/dL or INR ≥1.6 on postoperative day 7, or AST/ALT \>2000 IU/L within the first 7 postoperative days.

次要结局

未报告次要终点

研究者

发起方
The Mediterranean Institute for Transplantation and Advanced Specialized Therapies
申办方类型
Other
责任方
Sponsor

研究点 (14)

Loading locations...

相似试验