Recruiting

EAT with Semaglutide

Sponsor:

University of Virginia

Code:

NCT07178145

Conditions

Heart Failure Preserved Ejection Fraction

Epicardial Adipose Tissue

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

GLP-1RA

Study Details

Brief summary:

This study seeks to develop improved cardiac MRI (CMR) methods to quantify epicardial adipose tissue (EAT) composition and to demonstrate the advantages of EAT composition imaging (a) in advancing the understanding of the relationship between EAT and heart failure with preserved ejection fraction (HFpEF) and (b) for understanding mechanisms of and guiding medical therapy in HFpEF. The investigators recently developed the first method for quantifying EAT FAC in human subjects, utilizing a rate-6 accelerated radial 2D multi-echo gradient-echo breathhold acquisition with a local low rank reconstruction. In this project the first specific aim is to develop a rapid free-breathing 3D EAT FAC MRI method that reduces motion-related artifacts, increases coverage, and facilitates higher spatial resolution and improved FAC reproducibility. The second specific aim is to show that EAT FAC is more strongly associated than EAT volume with cardiometabolic HFpEF. In this context, individuals with known or suspected HFpEF will undergo CMR, echocardiography, and other testing to (a) diagnose cardiometabolic HFpEF; (b) characterize features associated with the severity of HFpEF; and (c) assess EAT volume and FAC. The investigators will determine if EAT FAC is more strongly associated than EAT volume with HFpEF and with features associated with the severity of HFpEF. The third specific aim is to show, in the context of cardiometabolic HFpEF and pre-HFpEF, (a) that GLP-1 receptor agonism with semaglutide (SEMA) shifts the EAT FAC to a less proinflammatory profile and (b) that baseline EAT FAC is a stronger predictor than EAT volume of improved cardiovascular function due to SEMA. Cardiometabolic HFpEF and pre-HFpEF subjects will undergo echocardiography and CMR with EAT FAC at baseline and after 3 months to serve as a self-control. Subjects will then undergo repeat imaging 6 months after the initiation of SEMA. The change in FAC after treatment with SEMA will be compared to the change in FAC prior to SEMA. Data will be analyzed to show that SEMA changes EAT FAC, and that baseline EAT FAC is a stronger predictor than EAT volume of improvements in severity of HFpEF.

Conditions

Heart Failure Preserved Ejection Fraction

Epicardial Adipose Tissue

Study ID

NCT07178145

Start date

Nov 20, 2025

Status verified date

Aug, 2026

Completion date

Dec, 2029

Anticipated

Primary completion date

Sep, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age ≥ 18 years - 90 years;
  • LVEF ≥ 50%;
  • ≥ 2 risk factors for HFpEF or symptoms that could be related to HFpEF (e.g., dyspnea, orthopnea, paroxysmal nocturnal dyspnea, lower extremity edema, pulmonary edema, etc);
  • Not currently being treated with GLP-1RA therapy.

Exclusion Criteria:

  • • Previously or currently reduced EF (<50%), including heart transplant; (2) Obstructive un-revascularized coronary disease by coronary CT or invasive coronary angiography;

  • MI/PCI/CABG within the past 6 months;
  • Untreated severe stenotic or regurgitant valvular disease;
  • Infiltrative cardiomyopathy (Fabry/HCM/sarcoid/amyloid, etc);
  • Myocarditis;
  • Claustrophobia/inability to tolerate MRI;
  • Implants that are a contraindication for MRI or may negatively impact image quality (e.g. pacemakers and ICDs);
  • Active systemic inflammatory disorder;
  • Atrial fibrillation with rapid ventricular response at time of study; and
  • Hemodynamic instability
  • Pregnancy
  • Prisoners
  • Inability to provide informed consent

Exclusion Criteria for Optional Cardiac Stress Imaging Procedure

  • allergy to gadolinium-based contrast agents
  • Acute kidney injury
  • Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m²
  • Hepatorenal syndrome
  • History of liver transplant
  • High-grade atrioventricular (AV) block
  • Active asthma exacerbation
  • Known allergy to vasodilator agents
  • Recent seizure

Study Design

Enrollment

192 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Diagnostic

Interventions and Outcome Measures

Arms

no intervention: 3D EAT FAC CMR imaging

non-contrast MRI to debug/test 3D MRI techniques for quantifying EAT FAC

no intervention: Imaging acquisition and medical condition overview

Will undergo Cardiac MRI, exercise echocardiography, 12 lead ECG, medical history review, bloodwork, physical exam, and optional stress cardiac MRI.

experimental: Imaging acquisition and GLP-1RA treatment

Will undergo all testing before and after a 6-month treatment of GLP-1RA

Interventions

GLP-1RA

Receive 6 months of GLP-1RA (Semaglutide) treatment starting at 0.25mg once weekly and then the dose will be up titrated as tolerated every four weeks to once-weekly doses of 0.5, 1.0, 1.7, and 2.4 mg until a maximum dose of 2.4mg (or the subject's maximally tolerated dose, if the subject's maximally tolerated dose is <2.4 mg) is reached after 16 weeks.

Primary outcome measure

  • Epicardial adipose tissue (EAT) fatty acid composition (FAC) [ Time Frame: Baseline, 3 months (self-control period), and 9-months (6 months post semaglutide treatment) ]

Central Contacts and Locations

Central contacts

Locations

University of Virginia

Recruiting

Charlottesville, Virginia, United States, 22903

Contacts

Principal Investigator:

Amit Patel, MD

More Information

Sponsor

University of Virginia

Last update posted

Aug 11, 2026

Last verified

Aug, 2026

Keywords

  • HFpEF
  • Heart Failure preserved Ejection Fraction
  • Cardiac MRI
  • Epicardial Adipose Tissue
  • GLP-1
  • EAT FAC
  • cardiovascular function

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Virginia on 2026-08-11.