Hypothermic Oxygenated Perfusion (HOPE) of Human Liver Grafts
Primary Purpose
Hepatocellular Injury
Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Hypothermic oxygenated perfusion (HOPE)
Sponsored by
About this trial
This is an interventional treatment trial for Hepatocellular Injury focused on measuring liver transplantation, machine liver perfusion, extended criteria liver grafts, donation after cardiac death, hypothermic machine liver perfusion, liver reperfusion injury
Eligibility Criteria
Inclusion Criteria:
- Adult (≥18 years) patients with acute liver failure or liver cirrhosis (CHILD A, B or C) and/ or malignant liver tumors requiring liver transplantation
- Whole liver graft
- Signed informed consent
Exclusion Criteria:
- Split graft
- Living donor liver transplantation
- Grafts donated after cardiac arrest (DCD grafts)
- Domino transplantation
- Combined liver transplant
- Cold storage > 15h
- acute and unexpected medical contraindication
Sites / Locations
- University Hospital of Zurich
- University of Zurich
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Hypothermic oxygenated perfusion (HOPE)
Control group: no intervention
Arm Description
Application of HOPE for 1 hour
Conventional cold storage (IGL-1)
Outcomes
Primary Outcome Measures
major complications after liver transplantation
post transplant complication Clavien >= III within 1 year after transplant
Secondary Outcome Measures
Laboratory parameters post transplant
Serum concentrations of bilirubin, AST, ALT, INR; Factor V
Cholangiopathy
Biliary complications
hospital stay, ICU stay
length of hospital and ICU stay after liver transplantation
Patient and graft survival
one year patient and graft survival
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01317342
Brief Title
Hypothermic Oxygenated Perfusion (HOPE) of Human Liver Grafts
Official Title
A Randomized Multicenter Study on the Effects of Hypothermic Oxygenated Perfusion (HOPE) on Human Liver Grafts Before Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
August 30, 2020 (Actual)
Study Completion Date
August 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is, in a randomized trial, to test a newly developed machine perfusion technique of human liver allografts before transplantation.
Ischemia-reperfusion injury is universal in organ transplantation and leads to varying degrees of graft dysfunction. Despite this fact, the preservation method in organ transplantation has been left unchanged for many years and remains simple static cold storage. Given the scarce donor supply, an increasing number of so called marginal or extended criteria donor organs have been used for liver transplantation, grafts which were previously rarely considered. In addition, allocation policy has changed in many countries, and livers are currently often distributed by the severity of the recipient's disease. As a result, transplant candidates present sicker, with higher MELD (Model for end stage liver disease) scores, at the time of transplant,and the risk of graft dysfunction or even failure due to reperfusion injury is high after the use of marginal livers in sick recipients.
Machine liver perfusion techniques have been significantly improved during the past decade to decrease reperfusion injury, and a number of promising results show beneficial effects in various animal transplant models by either normothermic or hypothermic oxygenated continuous liver perfusion. These techniques generally require machine liver perfusion immediately after organ procurement. However, continuous perfusion has several drawbacks, including major logistic efforts and risk of organ damage during perfusion and transport.
Our group, therefore, focused on the practicability of machine liver perfusion. We developed an endischemic hypothermic oxygenated perfusion (HOPE) concept through the portal vein only. This technique can be easily applied in the operation room shortly before transplantation of the recipient, thus after organ transport and back table preparation.
Recently, the beneficial effect of a similar approach has been confirmed in human liver grafts by a phase I non randomized trial. These results prove feasibility and safety of an endischemic hypothermic machine perfusion approach and warrant further randomized studies.
Detailed Description
The study consists on two groups, a perfusion group and a control group. Patients on the waiting list for liver transplantation with proven written consent will be recruited and randomized during organ procurement. Randomization will be performed by computer (secutrial). Perfusion will be started in the operation room after regular organ procurement, transport and back table preparation. The perfusion procedure will not delay the implantation due to the fact that recipient hepatectomy usually takes 2 hours. During this procedure, hypothermic oxygenated perfusion (HOPE group) for one hour will be performed vs continued cold storage (Control group).
We will use commercially available and approved IGL solution (Institut George Lopez) as perfusate for machine perfusion.
Subjects will be followed for one year after transplantation.
10 European centers are participating in this study, Randomization is stratified by center.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Injury
Keywords
liver transplantation, machine liver perfusion, extended criteria liver grafts, donation after cardiac death, hypothermic machine liver perfusion, liver reperfusion injury
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
179 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hypothermic oxygenated perfusion (HOPE)
Arm Type
Active Comparator
Arm Description
Application of HOPE for 1 hour
Arm Title
Control group: no intervention
Arm Type
No Intervention
Arm Description
Conventional cold storage (IGL-1)
Intervention Type
Device
Intervention Name(s)
Hypothermic oxygenated perfusion (HOPE)
Intervention Description
Application of HOPE for 1 hour, perfusion rate 150-300 ml/min, pressure controlled, perfusion pressure < 3 mm Hg, perfusion route portal vein, recirculating system, perfusion volume 2 L, perfusate Institute George Lopez solution (IGL-1), perfusate temperature 4-6 °C, perfusate oxygenation 150-200 mm Hg
Primary Outcome Measure Information:
Title
major complications after liver transplantation
Description
post transplant complication Clavien >= III within 1 year after transplant
Time Frame
During the first year postoperatively
Secondary Outcome Measure Information:
Title
Laboratory parameters post transplant
Description
Serum concentrations of bilirubin, AST, ALT, INR; Factor V
Time Frame
during first week, & 3,6,9,12 months
Title
Cholangiopathy
Description
Biliary complications
Time Frame
during 12 months after transplant
Title
hospital stay, ICU stay
Description
length of hospital and ICU stay after liver transplantation
Time Frame
during 12 months after transplant
Title
Patient and graft survival
Description
one year patient and graft survival
Time Frame
during 12 months after transplant
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult (≥18 years) patients with acute liver failure or liver cirrhosis (CHILD A, B or C) and/ or malignant liver tumors requiring liver transplantation
Whole liver graft
Signed informed consent
Exclusion Criteria:
Split graft
Living donor liver transplantation
Grafts donated after cardiac arrest (DCD grafts)
Domino transplantation
Combined liver transplant
Cold storage > 15h
acute and unexpected medical contraindication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philipp Dutkowski
Organizational Affiliation
Department of Surgery and Transplantation, University Hospital Zurich
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
Facility Name
University of Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
12. IPD Sharing Statement
Citations:
PubMed Identifier
19806056
Citation
de Rougemont O, Breitenstein S, Leskosek B, Weber A, Graf R, Clavien PA, Dutkowski P. One hour hypothermic oxygenated perfusion (HOPE) protects nonviable liver allografts donated after cardiac death. Ann Surg. 2009 Nov;250(5):674-83. doi: 10.1097/SLA.0b013e3181bcb1ee.
Results Reference
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PubMed Identifier
18416733
Citation
Dutkowski P, de Rougemont O, Clavien PA. Machine perfusion for 'marginal' liver grafts. Am J Transplant. 2008 May;8(5):917-24. doi: 10.1111/j.1600-6143.2008.02165.x.
Results Reference
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PubMed Identifier
17122622
Citation
Dutkowski P, Furrer K, Tian Y, Graf R, Clavien PA. Novel short-term hypothermic oxygenated perfusion (HOPE) system prevents injury in rat liver graft from non-heart beating donor. Ann Surg. 2006 Dec;244(6):968-76; discussion 976-7. doi: 10.1097/01.sla.0000247056.85590.6b.
Results Reference
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Hypothermic Oxygenated Perfusion (HOPE) of Human Liver Grafts
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