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New combo ablation aims to tame stubborn AFib

NCT ID NCT07633509

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jul 28, 2026 · Updated 2 times

Summary

This trial tests whether adding extra ablation lines to the standard pulsed-field ablation procedure helps people with long-standing atrial fibrillation (AF) stay in normal heart rhythm. 430 participants with AF lasting 1-3 years will be randomly assigned to receive either standard PFA or PFA plus additional radiofrequency and ethanol ablation. The main goal is to see if the more extensive procedure reduces AF recurrence at 12 months.

What this could mean

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

Active substance
Pulsed-field ablation and radiofrequency ablation catheters, plus ethanol infusion into the vein of Marshall
What this could lead to
If it works, this could lead to a more effective procedure that helps more people with long-standing atrial fibrillation stay in normal heart rhythm for longer.
What could go wrong
This is an early-stage trial with no results yet. The extra ablation may not improve outcomes and could increase procedure time or complication risks.

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 430 people

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

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Dec 2029

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 to 75 years

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 patients with long-standing persistent atrial fibrillation. * Duration of atrial fibrillation between 1 and 3 years. * Age 18 to 75 years. * Documentation of atrial fibrillation within 3 years prior to enrollment. * Willing and able to comply with the study protocol and provide written informed consent. Exclusion Criteria: * Paroxysmal atrial fibrillation, or evidence of sinus rhythm on electrocardiogram within the past year. * Persistent atrial fibrillation lasting less than 1 year or more than 3 years. * Left atrial thrombus. * Prior catheter ablation for atrial fibrillation. * Coexisting severe organic heart disease (e.g., severe valvular heart disease, hypertrophic cardiomyopathy, dilated cardiomyopathy, etc.). * Left atrial diameter (LAD) \>55 mm. * Left ventricular ejection fraction (LVEF) \<40%. * Known allergy or contraindication to low-molecular-weight heparin, warfarin, or direct oral anticoagulants. * Undergoing a "one-stop" procedure combining atrial fibrillation ablation with left atrial appendage closure. * Allergy to alcohol or contrast media. * Pulmonary artery systolic pressure \>50 mmHg. * Unstable angina pectoris. * Percutaneous coronary intervention (PCI) within the past 3 months. * Cardiac surgery within the past 6 months. * Planned heart transplantation. * History of thromboembolic disease within the past 6 months (including venous thromboembolism: pulmonary embolism, deep vein thrombosis; or arterial thromboembolic disease: acute coronary syndrome, lower extremity arterial embolism, stroke). * Left atrial myxoma. * Severe respiratory disease. * Active infectious disease. * Poorly controlled or active systemic immune disease (equivalent to glucocorticoid use \>2 tablets/day). * Unresolved malignant hematologic disease, or currently receiving chemotherapy, radiotherapy, or immunotherapy. * Unresolved malignant solid tumor, or currently receiving chemotherapy, radiotherapy, or immunotherapy. * Untreated hypothyroidism or hyperthyroidism. * Severe hepatic insufficiency (alanine aminotransferase \[ALT\] or aspartate aminotransferase \[AST\] \>3 times the upper limit of normal). * End-stage renal failure requiring dialysis. * Other serious arrhythmias, such as hemodynamically unstable ventricular tachycardia. * Pregnancy or breast-feeding. * Psychiatric disorder. * Body mass index (BMI) \<18.5 or \>35.0 kg/m². * Life expectancy \<2 years.

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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

    3 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

  • Beijing Anzhen Hospital, Capital Medical University

    Beijing, Beijing Municipality, 101118, China

  • Fuwai Hospital

    Beijing, Beijing Municipality, 100039, China

  • Jiangsu Province Hospital (The First Affiliated Hospital with Nanjing Medical University , Jiangsu Women and Children Health Hospital)

    Nanjing, Jiangsu, 210029, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.