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NCT06699342Recruiting

Pacing of Left Bundle Branch Area and Atroventricular Node ablatIon in Patients With Symptomatic Atrial Fibrillation

Source: ClinicalTrials.gov · Last updated 20 Aug 2026

Brief summary (registry, in English)

This study aimed to compare the clinical outcomes of left bundle branch area pacing combined with atrioventricular node ablation and pharmacologic treatment optimized according to guidelines in patients with symptomatic atrial fibrillation refractory or intolerant to drug therapy or catheter ablation.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
3 Nov 2024
Start date
27 Jan 2025
Primary completion date
31 Dec 2027
Lead sponsor
Seoul National University Hospital
NCT number
NCT06699342

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 27 Jan 2025 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Inclusion:
  • Patients who meet all of the following inclusion criteria 1)-6).
  • Permanent atrial fibrillation
  • Age ≥ 65 years
  • Refractory or intolerant to antiarrhythmic drugs, rate control medications, or catheter ablation
  • New York Heart Association (NYHA) functional class II- IV
  • LVEF \> 40% (within the past 3 months)
  • Patients with at least one of the following:
    • HF hospitalization (defined as HF as the major reason for hospitalization or treatment for HF lasting ≥12 hours and including treatment with intravenous (IV) diuretics at a healthcare facility) within 12 months
    • Elevated NT-proBNP (\>900 pg/ml) in the 30 days prior to enrollment
    • Exclusion:
    • Patients who meet at least one of the following exclusion criteria 1)-11).
  • Asymptomatic atrial fibrillation
  • Life expectancy to \< 12 months.
  • Primary moderate to severe valvular disease (except for functional mitral valve regurgitation or tricuspid valve regurgitation)
  • Mechanical tricuspid valve replacement
  • Severe chronic kidney disease (estimated Glomerular Filtration Rate ≤ 15 ml/1,73 m2 or receiving renal replacement treatment including hemodialysis or peritoneal dialysis)
  • Obstructive hypertrophic cardiomyopathy
  • Infiltrative cardiomyopathy (amyloidosis, sarcoidosis, Fabry disease, others)
  • Acute coronary syndrome or coronary revascularization (CABG or PCI) \<3 months
  • Severe primary pulmonary disease such as cor pulmonale, irreversible lung disease requiring inhalers, oxygen supplementation
  • Pacemaker/ICD/CRT treatment ongoing, or current pacemaker indication
  • Simultaneous participation in a different randomized clinical trial

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Seoul National University Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.