Two ways to quiet a racing heart: trial pits hybrid ablation against standard catheter treatment
NCT ID NCT05723536
First seen Sep 18, 2026 · Last updated Sep 18, 2026
Summary
Researchers compare two procedures for people with persistent atrial fibrillation that has not responded to at least one antiarrhythmic drug. One group receives standard catheter ablation, which burns or freezes small areas inside the heart. The other receives a hybrid procedure that combines keyhole surgery and a catheter to isolate more of the left atrium in a single session. The trial tracks heart rhythm over a year using an implanted monitor and uses MRI and echocardiography to see how heart structure affects success.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Partial left atrial isolation, a hybrid surgical and catheter procedure that electrically isolates parts of the left atrium
- What this could lead to
- If it works, this hybrid approach could give people with persistent atrial fibrillation a better shot at staying in normal rhythm than standard catheter ablation alone.
- What could go wrong
- The hybrid procedure is more invasive than catheter ablation and may carry extra risks. This is a small, single-center trial, so results may not apply broadly.
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
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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
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: 1. Patients between the ages of 18 and 75, both inclusive, at the time of the consent date. 2. Patients with persistent atrial fibrillation refractory to at least one antiarrhythmic drug (Class I or III). 3. Signature of written informed consent. Exclusion Criteria: 1. Continuous Persistent atrial fibrillation of more than 4 years. 2. Moderate to severe valvular heart disease. 3. Severe atrial dilatation (left appendage AP diameter \> 55 mm or \> 50ml/m2). 4. Patients requiring concomitant cardiac surgery or with previous cardiac surgery. 5. Left ventricular ejection fraction \<40%. 6. History of pericarditis. 7. Previous stroke. 8. Presence of active infection or sepsis, esophageal ulcer stricture and/or esophageal varices. 9. Patients with renal dysfunction defined as GFR less than or equal to 40 ml/min/m2. 10. Contraindication for chronic anticoagulation. 11. Patients who have undergone prior left atrial catheter ablation for atrial fibrillation or who are receiving treatment for ventricular arrhythmia. 12. Patients with severe chronic obstructive pulmonary disease considered GOLD III. 13. Patients with active neoproliferative disease or other concomitant disease where the medical team considers that ablation places the patient at unacceptable risk. 14. Pregnant, lactating women. 15. Patients who have previously presented allergic reactions to gadolinium. 16. Patients with claustrophobia that makes it impossible to perform nuclear magnetic resonance. 17. Persistent AF \< 3 months
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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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Hospital Clínic de Barcelona
RECRUITINGBarcelona, Spain
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