Enrolling now · NCT06499857

A study testing whether a GLP-1 medicine from University of Chicago, semaglutide, can help with weight.

What this means for you

Who can join
Adults 18 to 75, have obesity or are overweight, BMI 30+.
What you take
semaglutide, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
How long it lasts
The full study runs about 3.2 years; your own time in it is usually shorter.
What you get
The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
Phase Phase 3Sponsor University of ChicagoDrug semaglutideClass GLP-1 RASites 2 USEnrollment target 200

What this study is for

Primary condition: Overweight or Obesity. Also studied in: Atrial Fibrillation.

Full scientific study title: Semaglutide for Metabolic Intervention and Adipose Loss to Treat Atrial Fibrillation.

Who can join

Age18 to 75SexAnyBMI30 or higher

Adults 18 to 75, have obesity or are overweight, BMI 30+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • Age 18-75 years
  • BMI greater than or equal to 30 kg/m2
  • Paroxysmal AF or persistent AF, in whom catheter ablation (CA) for AF is expected within 1 year (A group) or in whom catheter ablation is NOT expected within 1 year (M group)
  • Ability to provide informed consent before any trial-related activities.
  • Patients with type 2 diabetes mellitus (T2DM) will be included:

Key exclusion criteria

  • Current use of GLP-1 RA (glucagon-like peptide receptor agonists) or DPP4 (Dipeptidyl peptidase-4)-inhibitors or use within the last 90 days prior to screening
  • Current antiobesity medication use or use within the last 90 days prior to screening
  • A self-reported change in body weight of > 5 kg (11 lb.) within 30 days before screening
  • History of bariatric surgery
  • History of type I diabetes mellitus

Where this study is enrolling

This trial has 2 sites across 2 states. Contact a site coordinator directly to start screening.

Arizona1 site
  • The University of Arizona College of Medicine- Phoenix
    Phoenix, Arizona
    Roderick Tung, MD602-521-3090rodericktung@arizona.edu
Illinois1 site

Timeline

Started enrolling: 2025-04-14. Expected completion: 2028-06. Last updated on ClinicalTrials.gov: 2025-11-14.

Official source

We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:

View on ClinicalTrials.gov →

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