Using Ex-vivo Normothermic Machine Perfusion With the Organox Metra™ Device to Store Human Livers for Transplantation

Last updated: April 8, 2022
Sponsor: University Health Network, Toronto
Overall Status: Active - Enrolling

Phase

1

Condition

Liver Failure

Primary Biliary Cholangitis

Treatment

N/A

Clinical Study ID

NCT02478151
14-8132-B
  • Ages 18-70
  • All Genders

Study Summary

This trial will examine the safety and feasibility of using the OrganOx Metra device to transport and store donor livers under normothermic conditions prior to transplantation. Participants will be followed for 3 months following transplantation and their outcomes recorded.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult patients (18 years or more)
  • Active on the waiting list for liver transplantation
  • Able to give informed consent

Exclusion

Exclusion Criteria:

  • Age less than 18 years
  • Acute/fulminant liver failure
  • Transplantation of more than one organ (e.g. liver and kidney)
  • Refusal of informed consent
  • Unable to give informed consent
  • Re-transplantation Diagnosis of Hepatopulmonary Syndrome

Study Design

Total Participants: 40
Study Start date:
July 01, 2015
Estimated Completion Date:
March 31, 2023

Study Description

Liver transplantation is a life-saving procedure but its success has been limited by a shortage of suitable donor organs. Much emphasis is now placed on optimising the condition of those organs that are available, to enable more higher risk organs to be transplanted safely. An effective means of pre-transplant viability assessment would not only allow greater use of higher risk donors but also minimise the risk of primary non-function by identifying and excluding non-viable organs before subjecting a patient to the risk of surgery. Organ storage under normothermic perfusion conditions enables organ function to be evaluated prior to transplantation and further has been shown to prevent organ injury which is sustained during standard cold storage. This trial will examine the safety and feasibility of using the OrganOx Metra device to transport and store donor livers under normothermic conditions prior to transplantation. This study will evaluate liver function post-transplantation using standard clinical parameters. Participants will be followed for 3 months following transplantation and their outcomes recorded. Participants will undergo no other study procedures. Feasibility will be measured using the ratio of actual / eligible candidate donors recruited to the study and will also encompass logistical issues with respect to transportation, and ease of use. Safety will be assessed by rates of device failures resulting in organ discard, primary graft non-function, re-transplantation, and recipient death.

Connect with a study center

  • Toronto General Hospital

    Toronto, Ontario M5G 2N2
    Canada

    Site Not Available

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