Skip to content
Clinical Trials – home

Arrhythmia Trials in Disease

1 / 2 trials open to patients2 countries

In short

This article provides information about 2 ongoing clinical trials focused on supraventricular arrhythmia, specifically atrial fibrillation and atrial arrhythmia. These studies are investigating different medications to help manage irregular heartbeats and improve heart rhythm in patients with these conditions. Trials are currently taking place in the Netherlands and France.

Clinical trial locations

Study on Semaglutide for Achieving Sinus Rhythm in Patients with Obesity and Persistent Atrial Fibrillation

This trial is investigating whether Semaglutide can help restore a normal heart rhythm in people who have both obesity and persistent atrial fibrillation. Atrial fibrillation is a condition where the heart beats irregularly, which can lead to various complications including poor blood flow and increased risk of blood clots.

Who can participate: You may be eligible if you are 18 years or older and have symptomatic, first-detected persistent atrial fibrillation that was noticed for the first time within the past 6 months. You must also have obesity, which means a Body Mass Index of 30 or higher, or a BMI of 27 or higher if you have other weight-related health issues like high blood pressure, high cholesterol, sleep problems, or heart disease. You need to be scheduled for electrical cardioversion, a procedure to help restore normal heart rhythm, and must provide written informed consent.

Who cannot participate: The study excludes patients who do not have obesity or atrial fibrillation. You also cannot join if you are outside the specified age range or if you are part of a vulnerable population that may need special protection or care.

What the trial involves: Participants receive either Semaglutide or a placebo as a weekly injection under the skin for one year. Semaglutide is a medication that helps control weight by mimicking a hormone called GLP-1, which regulates appetite and insulin levels. Throughout the study, researchers monitor changes in heart rhythm, symptoms of atrial fibrillation, quality of life, weight, blood pressure, cholesterol levels, and the number of hospital visits. The main goal is to see if Semaglutide can help patients achieve and maintain a normal heart rhythm while also addressing obesity-related health issues.

Study on Flecainide to Reduce Risk of Atrial Arrhythmia After Patent Foramen Ovale Closure in Patients

This trial examines whether Flecainide can prevent irregular heartbeats in patients who have undergone a procedure to close a patent foramen ovale (PFO), which is a small opening in the heart that didn't close naturally after birth. Sometimes after this closure procedure, patients can develop atrial arrhythmias or tachycardia, which are irregular or fast heartbeats.

Who can participate: You may be eligible if you are 18 years or older and are a candidate for PFO closure. The need for this procedure must be confirmed by a team of medical experts. You must be affiliated with Social Security and have provided signed written consent. Additionally, you must have had a successful PFO closure without any major complications.

Who cannot participate: You cannot join this study if you have a history of atrial arrhythmia or tachycardia before the PFO closure procedure. Individuals outside the specified age range and those who are part of vulnerable populations are also excluded.

What the trial involves: After the PFO closure procedure, a small device called an Insertable Cardiac Monitor (ICM) is implanted to continuously track heart activity. Participants then receive Flecainide, an oral medication taken in tablet form, for three months. Flecainide works by blocking sodium channels in the heart, which helps stabilize the heart's rhythm and is classified as a Class IC antiarrhythmic agent. Researchers monitor participants for six months in total, looking for any episodes of irregular heartbeats (including those with and without symptoms), palpitations, strokes, unexpected medical visits, and any side effects from the medication. The primary focus is on whether Flecainide can reduce the occurrence of atrial arrhythmia during the first three months after the PFO closure.

Summary

These two clinical trials represent different approaches to managing supraventricular arrhythmias. The first study in the Netherlands focuses on addressing atrial fibrillation in patients with obesity using Semaglutide, a medication primarily known for weight management that may also help restore normal heart rhythm. The second trial in France investigates the preventive use of Flecainide, a traditional antiarrhythmic medication, to reduce the risk of irregular heartbeats after a heart procedure.

Both studies use modern monitoring technology to carefully track heart rhythm and assess the effectiveness and safety of their respective treatments. While the trials address different patient populations and use different medications, they share the common goal of improving heart rhythm management and reducing complications associated with atrial arrhythmias.

This guide is here to help you understand the condition. It does not replace a conversation with your doctor, who knows your situation best.

Clinical trials for Arrhythmia

Recruiting trials first

See all 2 trials →
Quick filters

2 clinical trials in this condition

Countries:The NetherlandsThe Netherlands
  • Participants:18–64 years · 65+ years
  • Substances:Atenolol
  • Sponsor:Amsterdam UMC

Arrhythmia

Not recruiting
Registered drug
Countries:FranceFrance
  • Participants:18–64 years · 65+ years
  • Substances:Flecainide
  • Sponsor:Assistance Publique Hopitaux De Paris
See all 2 trials →filters applied: condition = Arrhythmia

Related conditions in the same therapeutic area

Back to all diseases
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

© 2026 Clinical Trials EU – European Clinical Trials Information Network

GDPR compliance, ISO 9001 and ISO 27001 certified (LL-C Certification)

On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).