Abdominal Regional Perfusion in Donation After Cardiac Death for Multi-Organ Transplantation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorLondon Health Sciences Centre

About this trial

The main purpose of this study is to increase the pool of organs available for donation by performing ARP to recondition donation after cardiac death (DCD) organs prior to transplantation. We will compare the outcomes of our ARP DCD liver transplants with historical data to determine the efficacy of this treatment compared to transplantation with standard DCD and donation after brain death (DBD) organs. We will also analyze biological samples from donors and recipients and compare them with outcome data in an effort to determine if any biological markers are able to predict the quality/success of the grafts.

Eligibility criteria

Qualifiers

Indications for Liver transplant include decompensated Cirrhosis of any etiology Model for End-Stage Liver Disease (MELD) score > 15 with no contraindications to liver transplant as per conventional clinical practice.

Disqualifiers

Inadequate social support for liver transplant

Non-compliance with alcohol or narcotic cessation

Evidence of uncontrolled infection

Other untreated malignancy aside from those listed above

Trial design

Treatments tested in this trial

  • Abdominal Regional Perfusion

Treatment groups

20 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators