Actively Recruiting

Phase Not Applicable
Age: 19Years +
All Genders
NCT05794386

SCAR Burden of Left Atrium Guided cathEter Ablation sTrategy for Persistent Atrial Fibrillation

Led by Seoul National University Hospital · Updated on 2026-04-28

204

Participants Needed

1

Research Sites

256 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a multicenter, randomized controlled trial to compare the recurrence of 1-year atrial arrhythmia after catheter ablation of atrial fibrillation (AF) between pulmonary vein isolation (PVI) and PVI with additional left atrial (LA) substrate modification based on the left atrial low-voltage area (LA LVA) in patients with persistent AF who had a moderate burden of LVA in LA (1cm2 to \<30%).

CONDITIONS

Official Title

SCAR Burden of Left Atrium Guided cathEter Ablation sTrategy for Persistent Atrial Fibrillation

Who Can Participate

Age: 19Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 19 years or older
  • Symptomatic persistent atrial fibrillation continuing despite anti-arrhythmic drugs
  • Left atrial low-voltage area (LVA) between 1cm2 and less than 30% on 3D voltage mapping
  • Patients with LVA less than 1cm2 or 30% or more are included in a registry but not randomized
Not Eligible

You will not qualify if you...

  • Left atrial anteroposterior diameter greater than 55 mm
  • Prior catheter ablation or surgery for atrial fibrillation
  • Inability to obtain high-quality 3D voltage mapping or calculate exact LVA burden
  • Inability or unwillingness to use anticoagulation treatment
  • Severe left ventricular dysfunction (ejection fraction less than 35%)
  • Severe structural heart disease including severe mitral regurgitation, hypertrophic cardiomyopathy, or other severe valve disease
  • Presence of intracardiac thrombus
  • Prior cardiac surgery
  • Myocardial infarction or coronary intervention within 3 months
  • Stroke or transient ischemic attack within 6 months
  • Planned cardiovascular surgery or procedure
  • Uncontrolled hypertension or thyroid disease
  • Need for dialysis or scheduled dialysis
  • Current pregnancy or pregnancy likely during study
  • Use of immunosuppressive drugs or recent chemotherapy
  • Life expectancy less than 1 year

AI-Screening

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Trial Site Locations

Total: 1 location

1

Seoul National University Hospital

Seoul, Jongno-gu, South Korea, 03080

Actively Recruiting

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Research Team

E

Eue-Keun Choi, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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