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Clinical Trials/NCT04023773
NCT04023773Active, not recruitingNot Applicable

Assess Safety and Feasibility of Sequential Hypothermic Oxygenated Machine Perfusion and Normothermic Machine Perfusion to Preserve Extended Criteria Donor Livers for Transplantation

Koji Hashimoto1 site in 1 country18 target enrollmentStarted: May 1, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
18
Locations
1
Primary Endpoint
graft survival at 1 month post-transplant

Study Overview

Brief Summary

Hypothermic machine perfusion (HMP) has been shown to be beneficial to preserve extended criteria donor (ECD) livers for transplantation. Normothermic machine perfusion (NMP) had the same benefits and also the convenience on liver quality assessment. The investigators proposed to do sequential HMP (1-4 hours) and NMP (1-14 hours) on 18 ECD transplanted human livers by using an institutional-developed perfusion device for liver transplantation.

Detailed Description

Liver transplantation is a successful therapy on the patients with end-stage liver disease, however is limited by the shortage of donor organs. Donor criteria were expanded in the past decades, however the extended criteria donor (ECD) livers may induce a higher risk of complications. Static cold storage (SCS) is the standard procedure for ex vivo liver preservation for about 4 decades, but has the limitation on preserving ECD livers and especially the inconvenience to evaluate liver quality prior to transplantation. Hypothermic (4-8 Celsius degree) machine perfusion (HMP) and Normothermic (35-37 Celsius degree) machine perfusion (NMP) have been shown to be beneficial to preserve extended criteria donor (ECD) livers respectively. NMP also had the convenience on liver quality assessment. The investigators had an institutional-developed device for liver NMP used on 25 patients with the FDA's IDE approval. In the present study the investigators are proposing to expand the use of the device on sequential HMP (1-4 hours) and NMP (1-14 hours) on 18 ECD transplanted human livers. This will be a single center prospective pilot study. The liver metabolism and hydrodynamics during perfusion will be recorded. The transplant procedure and post-transplant care will follow the clinical standard of care. The follow-up period is 12 months after transplantation. The primary end point will be the rate of patient survival and primary non function (PNF) within 30 days after transplantation, while the secondary end points will be: Early Allograft Dysfunction (EAD), 6 months patient and graft survival, peak liver function tests in the first 7 days after transplantation, surgical outcomes (operative time, transfusion requirement etc.), rate of post-transplant kidney failure, assessment of histological ischemia reperfusion (liver and bile duct), rate of vascular complications, rate of biliary complications, hospital and ICU length of stay, rejection rate, infection rate, the ability to predict function based on "on-pump" viability markers, and the incidence of adverse effect (AE).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients undergoing liver transplantation
  • Age 18 or older at the time of transplantation
  • Willingness and ability to comply with the study procedures
  • Signed Informed Consent Form

Exclusion Criteria

  • Recipient of partial grafts (split and living donors)
  • Mentally or legally incapacitated subjects
  • Inability to understand the procedures due to language barriers
  • Multiorgan transplant

Arms & Interventions

Liver perfusion

Experimental

Device: Liver Machine Perfusion (MP) Device

The liver grafts will be preserved at hypothermic and normothermic temperature on the institutional-developed Liver MP Device, and have continuous perfusion with oxygen supply in the ex vivo organ preservation phase.

Intervention: Liver Machine Perfusion (MP) device (Device)

Outcomes

Primary Outcomes

graft survival at 1 month post-transplant

Time Frame: 1 month post-transplant

graft survival will be recorded at 1 month post transplantation. The allograft will be considered lost if a patient has a primary non function (PNF), liver re-transplant or in the event of patient death.

patient survival at 1 month post-transplant

Time Frame: 1 month post-transplant

Patient survival will be recorded at 1 month post transplantation.

Secondary Outcomes

  • patient survival at 6 month post-transplant(6 month post-transplant)
  • graft survival at 6 month post-transplant(6 month post-transplant)
  • total bilirubin on post-operative day 7(on post-operative day 7)
  • international normalized ratio on post-operative day 7(on post-operative day 7)
  • ICU length of stay(up to 36weeks)
  • rate of post-transplant early allograft dysfunction (EAD)(in the first 7 days after transplantation)
  • peak alanine aminotransferases in the first 7 days after transplantation(in the first 7 days after transplantation)
  • peak aspartate aminotransferases in the first 7 days after transplantation(in the first 7 days after transplantation)
  • Hospital length of stay(up to 36 weeks)
  • Estimated blood loss at transplant surgery(during surgery)

Investigators

Sponsor
Koji Hashimoto
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Koji Hashimoto

Staff Physician

The Cleveland Clinic

Study Sites (1)

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