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临床试验/ACTRN12624000995572
ACTRN12624000995572尚未招募Unknown

Evaluate the Feasibility and Safety of Transplantation of Unsuitable Livers following Long-term Normothermic Perfusion for Adult Liver Transplant Recipient

Sydney Local Health District0 个研究点目标入组 54 人开始时间: 2024年8月14日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
入组人数
54

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
All

入选标准

  • Suitable potential LT-NMP trial graft recipients will be identified during their assessment and listing process. Eligible patients will be informed that they would be suitable to receive a graft from the NEOP trial. They will be given the patient information sheets to read more about the trial. If already listed, potential recipients will be identifiedt, contacted and sent the information documents. Informed consent will be obtained from all participants. Enrolling in the trial will not impact the chance of them receiving a standard ‘transplantable’ graft. Patients with all aetiologies of chronic liver disease will be considered for inclusion.
  • Recipients will meet all the following inclusion criteria to be eligible for participation in the NEOP trial:
  • Adult primary liver transplant recipient.
  • Patient listed electively (not ‘super-urgent) for transplantation.
  • Low to moderate transplant risk candidate, suitable for extended criteria grafts, as assessed by the ANLTU liver transplant listing multidisciplinary team (MDT) meeting (these are usually candidates with MELD score < 20, without cardiovascular comorbidities, with good functional and nutrition status, with patent portal vein and with no history of previous major upper abdominal surgery, for example, patients transplanted for liver cancer).
  • Able to undergo the informed consent process.

排除标准

  • Recipient exclusion criteria
  • Subjects who meet any of the following exclusion criteria are excluded from participating in the NEOP trial:
  • ‘High-risk patients’ not considered suitable for a marginal graft (these are mainly patients with high MELD score (>20) with cardiovascular comorbidities or renal insufficiency, with poor nutrition and performance status).
  • Patients with extensive portal vein thrombosis diagnosed prior to the transplantation.
  • Liver re-transplantation.
  • Patients with fulminant hepatic failure.
  • Patients undergoing transplantation of more than one organ.

研究者

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