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Search / Trial NCT04869813

Sarcopenia Magnetic Resonance Imaging Evaluation (SUSIE)

Launched by THE CLEVELAND CLINIC · Apr 28, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The SUSIE trial is looking to study a new imaging technique called Magnetic Resonance (MR) Fingerprinting and another method called Phosphorus-31 MR Spectroscopy (P-MRS). These methods will help researchers understand the muscles of people with heart failure, especially those who also have a condition called sarcopenia, which is the loss of muscle mass and strength. By comparing heart failure patients with and without sarcopenia, the trial aims to create detailed profiles of their muscle characteristics.

To be eligible for the trial, participants need to be at least 40 years old and have stable chronic heart failure with specific heart function issues. Healthy volunteers without heart failure or sarcopenia can also take part. However, there are some health conditions and medical devices that may disqualify individuals from participating, especially if they have advanced diseases or certain implants that are not safe for MRI scans. Participants will undergo MRI scans to gather important information about their muscle health, which may help improve treatments for heart failure in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Heart failure patients
  • Age ≥40 yrs
  • Stable chronic heart failure
  • Systolic dysfunction determined by cardiac MRI with left ventricle ejection fraction 40% or less
  • Healthy Volunteers
  • Age ≥40 yrs
  • No diagnosed heart failure or sarcopenia
  • Exclusion Criteria:
  • Heart failure patients
  • • Advanced liver disease, advanced cancer, advanced chronic obstructive pulmonary disease
  • Healthy volunteers (controls)
  • Advanced liver disease, advanced cancer, advanced chronic obstructive pulmonary disease
  • Contraindications to MRI Contraindications to MRI
  • Heart pacemaker/defibrillator
  • Electronic/implanted stimulators or devices, including deep brain stimulator, vagus nerve stimulator, bladder stimulator, spine stimulator, neurostimulators; implanted electrodes or wires
  • Cochlear implant or other ear implants
  • Implanted drug pumps (insulin, narcotic/pain medications, drugs to treat spasticity)
  • Programmable shunt
  • Aneurysm clips and coils
  • Stents
  • Filters (for example, blood clot filters)
  • Metal fragment in body or eye (eg, BBs, bullets, shrapnel, metal pieces or shavings)

About The Cleveland Clinic

The Cleveland Clinic is a renowned nonprofit academic medical center based in Cleveland, Ohio, recognized for its commitment to advancing healthcare through innovative research and clinical excellence. As a leading sponsor of clinical trials, the Cleveland Clinic leverages its multidisciplinary expertise and state-of-the-art facilities to conduct groundbreaking studies aimed at improving patient outcomes across a wide range of medical conditions. With a strong emphasis on patient-centered care, the institution fosters collaboration among researchers, clinicians, and patients to explore new treatments and therapies, contributing significantly to the global body of medical knowledge.

Locations

Cleveland, Ohio, United States

Patients applied

0 patients applied

Trial Officials

W. H. Wilson Tang, MD

Principal Investigator

The Cleveland Clinic

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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