Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05477277

Adverse Outcomes and Mortality in Liver Transplant Using MRI-Based Muscle Assessment Score

Led by Mayo Clinic · Updated on 2025-08-15

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

M

Mayo Clinic

Lead Sponsor

A

Amra Medical AB

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to explore the relationship between muscle composition, measured by an MRI-based Muscle Assessment Score (MAsS), and negative outcomes in people being evaluated for liver transplant. Sarcopenia, or loss of muscle volume and function, is common in end-stage liver disease and is linked to worse health outcomes and higher risk of death. The study also seeks to understand how muscle health interacts with donor liver characteristics to affect transplant success and survival. Participants will undergo MRI scans during their liver transplant evaluation, where the MAsS will be added to the standard MRI to assess muscle volume and fat infiltration. This score combines measures of muscle size and fat content to provide a detailed picture of muscle health. The study will use these MRI assessments to identify patients at high risk of adverse outcomes, both before and after transplant, over a one-year period. During the study, participants' muscle health and transplant outcomes will be monitored through MRI and clinical follow-up for one year. Researchers will evaluate changes in the MAsS while waiting for transplant and record adverse events and mortality. This approach aims to provide a standardized, objective measurement to better predict risks in liver transplant candidates and improve understanding of factors impacting transplant success.

CONDITIONS

Brief Title

Adverse Outcomes and Mortality in Liver Transplant

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with end-stage liver disease undergoing evaluation for liver transplant
  • Patients clinically indicated for MRI during transplant candidacy evaluation
  • Adults aged 18 years or older
Not Eligible

You will not qualify if you...

  • Contraindication to MRI scan preventing safe participation in imaging procedures

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) during transplant candidacy evaluation involving MRI scan

Diagnostic Evaluation

Duration - Up to 1 year while waiting for liver transplant

Participants undergo MRI-based muscle assessment as part of their standard transplant evaluation to measure muscle volume and fat infiltration using the Muscle Assessment Score (MAsS).

MRI scans as clinically indicated during transplant candidacy evaluation and follow-up

Long-term Monitoring

Duration - 1 year post-transplant

Participants are monitored for adverse outcomes and mortality for up to one year after liver transplant, including assessment of the association between muscle composition and transplant outcomes.

Follow-up visits as part of routine clinical care; additional assessments may occur depending on clinical indications

Trial Site Locations

Total: 1 location

1

Mayo Clinic Arizona

Phoenix, Arizona, United States, 85259

Actively Recruiting

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Research Team

L

Latasha Bunkley

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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Anette Karlsson, Johannes Rosander, Thobias Romu...

https://pubmed.ncbi.nlm.nih.gov/25111561

On the Definition of Sarcopenia in the Presence of Aging and Obesity-Initial Results from UK Biobank.

Jennifer Linge, Steven B Heymsfield, Olof Dahlqvist Leinhard

https://pubmed.ncbi.nlm.nih.gov/31642894

Adverse muscle composition is linked to poor functional performance and metabolic comorbidities in NAFLD.

Jennifer Linge, Mattias Ekstedt, Olof Dahlqvist Leinhard

https://pubmed.ncbi.nlm.nih.gov/33598647