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New heart procedure may leave hidden marks on the brain

NCT ID NCT07363278

Knowledge-focused Sponsor: Seoul National University Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study watches 40 adults with atrial fibrillation who get a new type of heart treatment called pulsed field ablation. The goal is to see if the procedure causes tiny, symptom-free brain spots that show up on MRI scans. Researchers want to know how often these spots happen and how big they are.

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.

Participants

About 40 people

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

Started

Dec 2025

Expected to finish

Dec 2027

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.

Who is studied

This study is designed as a registry to evaluate safety without a control group. The target sample size was determined with reference to previous studies that assessed the incidence of silent cerebral lesions (SCLs) using post-procedural MRI, in which approximately 30 to 40 patients were typically included.

Ages

19 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: 1\) Patients undergoing atrial fibrillation ablation using the Varipulse™ catheter Exclusion Criteria: 1. Individuals under 19 years of age 2. Patients who undergo concomitant radiofrequency ablation of the left atrium during the procedure 3. Patients with a history of stroke or transient ischemic attack (TIA) 4. Patients who have previously undergone ablation or surgery for atrial fibrillation 5. Patients with intracardiac thrombus or embolic events within the past 90 days 6. Patients who have experienced cardiac surgery or acute coronary syndrome within the past 90 days 7. Patients with contraindications to oral anticoagulant therapy, or those who require temporary discontinuation of anticoagulation due to procedural complications (e.g., cardiac tamponade) 8. Patients with a left ventricular ejection fraction (LVEF) of less than 35% 9. Women who are currently pregnant or planning to become pregnant during the study period 10. Patients with a life expectancy of less than one year 11. Patients at increased risk during MRI scanning (e.g., those with pacemakers or other metallic implants affected by MRI, or those with severe claustrophobia)

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Conditions

The condition(s) this trial relates to.

atrial fibrillation

As listed by the trial registrant

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

Atrial fibrillation (AF)

How to take part

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

  1. The places running it

    1 site. 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

  • Seoul National Universtiy Hospital, Seoul

    RECRUITING

    Seoul, Jongro-ku, 03080, South Korea

More trials for these conditions

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