Can shedding pounds stop atrial fibrillation in its tracks?

NCT ID NCT07816744

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time

Summary

Researchers in Denmark are testing whether a structured weight loss program can slow the progression of atrial fibrillation in people who are overweight or obese. The trial enrolls 480 adults with symptomatic paroxysmal or early persistent atrial fibrillation and a body mass index of at least 27. Participants are randomly assigned to either a comprehensive weight loss program with behavioral support, meal replacement, and optional GLP-1 medication, or to standard care alone. Everyone receives guideline-based heart care, and researchers track heart rhythm over 14-day monitoring periods for one year.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A structured weight loss program combining behavioral support, meal replacement, and the GLP-1 drug semaglutide
What this could lead to
If it works, this could give doctors a clear weight-loss strategy to slow atrial fibrillation and reduce symptoms in people with obesity.
What could go wrong
Weight loss is hard to maintain, and the trial may not show that it changes atrial fibrillation. GLP-1 drugs can cause nausea and other side effects, and the follow-up is only one year.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 480 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Sep 2030

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion criteria: * Symptomatic paroxysmal\* or persistent\*\* AF * Sinus rhythm at inclusion (Visit 1) * BMI ≥27 kg/m2 * Age\>18 years * At least one 12-lead ECG or other single- or multiple-lead ECG device (e.g. Holter monitor-ing or ECG-providing wearables) documented episode during 6 months prior to inclusion \* Paroxysmal AF in this trial is defined as at least 2 episodes, either self-terminating or cardioverted within 7 days, during 6 months prior to in-clusion \*\*Persistent AF in this study is defined as the following: * Duration of an AF episode \>7 days and \< 6 months * Total documented AF history \< 5 years Exclusion criteria: * Atrial flutter as the primary arrhythmia. (Patients with previous or isolated episodes of atrial flutter may be included, provided that AF is the dominant arrhythmia and the primary target of clinical management) * Implanted electronic device (pacemaker/ICD/ICM) * Type 1 diabetes or Type 2 diabetes on insulin treatment * Severe heart failure (LVEF \<40%) * Inability to sign informed consent * Severe kidney disease (eGFR\<30) * History of catheter ablation for AF * Scheduled to receive catheter ablation for AF during the study period (next 1 year) * Incretin-based therapy (GLP-1 receptor agonists or DPP-IV inhibitors) within 30 days prior to randomization (visit 1) * Scheduled for bariatric surgery during the study period * Hypertrophic cardiomyopathy, ARVC/D, non-compaction or amyloidosis * Chronic or previous acute pancreatitis * Current participation in any other clinical intervention trial that may result in changes to med-ical management during the study period * Women of childbearing potential who are not on an acceptable form of contraception * Pregnant or breastfeeding women * Personal or family history of medullary thyroid carcinoma (MTC) * History of MEN2 (Multiple Endocrine Neoplasia type 2)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Esbjerg Hospital - University Hospital of Southern Denmark

    Esbjerg, 6700, Denmark

  • University Hospital Bispebjerg and Frederiksberg

    Copenhagen, Denmark

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