Prediction of Donor Liver Adipose Content by Magnetic Resonance Imaging
Primary Purpose
Fatty Liver, Steatosis of Liver
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
MRI of donor liver prior to transplant
Sponsored by
About this trial
This is an interventional diagnostic trial for Fatty Liver focused on measuring transplantation, liver
Eligibility Criteria
Inclusion Criteria:
- Patients who are scheduled to orthoptic liver transplant
Exclusion Criteria:
- Patient's who do not agree to sign consent
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MRI of donor liver
Arm Description
MRI evaluation of graft steatosis in donor liver prior to transplantation
Outcomes
Primary Outcome Measures
Percent Hepatic Steatosis of a Donor Liver Prior to Transplantation
Amount of fat measured in the donor liver prior to transplant surgery using MRI scan
Secondary Outcome Measures
Comparison of steatosis percentages provided by biopsy to MRI results
Length of hospitalization of transplant recipient
Mortality of liver transplant recipient at 1 year post transplantation
Full Information
NCT ID
NCT02873507
First Posted
August 4, 2016
Last Updated
January 31, 2018
Sponsor
Vanderbilt University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT02873507
Brief Title
Prediction of Donor Liver Adipose Content by Magnetic Resonance Imaging
Official Title
Pilot Study for the Prediction of Donor Liver Adipose Content by Magnetic Resonance Imaging
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of funding
Study Start Date
May 2018 (Anticipated)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A pilot prospective cohort study assessing the clinical utility of MRI evaluation of graft steatosis prior to transplantation will be conducted. An MRI of the donor liver within the transport cooler will be obtained on its way to the operating room.
Detailed Description
The images from MRI will be analyzed to obtain information of fat content in all eight segments of the liver. Demographic, intra-operative, and post-operative patient data will be collected for each imaged graft.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatty Liver, Steatosis of Liver
Keywords
transplantation, liver
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MRI of donor liver
Arm Type
Experimental
Arm Description
MRI evaluation of graft steatosis in donor liver prior to transplantation
Intervention Type
Other
Intervention Name(s)
MRI of donor liver prior to transplant
Intervention Description
MRI of the on ice donor liver within the transport cooler on its way to the operating room
Primary Outcome Measure Information:
Title
Percent Hepatic Steatosis of a Donor Liver Prior to Transplantation
Description
Amount of fat measured in the donor liver prior to transplant surgery using MRI scan
Time Frame
Measured immediately prior to liver transplant
Secondary Outcome Measure Information:
Title
Comparison of steatosis percentages provided by biopsy to MRI results
Time Frame
Baseline
Title
Length of hospitalization of transplant recipient
Time Frame
Days to hospital discharge, approximately 2 weeks
Title
Mortality of liver transplant recipient at 1 year post transplantation
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who are scheduled to orthoptic liver transplant
Exclusion Criteria:
Patient's who do not agree to sign consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bret D Alvis, M.D.
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Prediction of Donor Liver Adipose Content by Magnetic Resonance Imaging
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