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Study identifier: NCT07250529 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Left Bundle Branch Pacing vs Right Ventricular Pacing on AHRE Burden in Patients With Preserved LVEF

Condition: Atrial Fibrillation (AF) · Pacemaker Therapy · Atrioventricular Block  ·  Sponsor: University Hospital of Patras

PhaseNA
Planned participants244
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This prospective, randomized controlled trial aims to evaluate the effect of left bundle branch pacing (LBBP) compared with conventional right ventricular (RV) pacing on the cumulative duration (total time) of atrial high-rate episodes (AHREs) in patients with preserved left ventricular ejection fraction (LVEF) who are expected to require frequent ventricular pacing. Atrial High-Rate Episodes (AHREs) are defined as episodes of atrial tachyarrhythmia that are automatically recorded by device diagnostics and detected by implanted cardiac devices. These episodes usually have an atrial rate ≥170 beats per minute and a duration ≥6 minutes. AHREs are linked to a higher risk of thromboembolic events and clinical atrial fibrillation (AF), and they may indicate subclinical AF or other atrial tachyarrhythmias. Chronic RV pacing has been linked to mechanical and electrical dyssynchrony, which may encourage atrial remodeling and the development of AF. LBBP provides a more physiological ventricular activation and may reduce atrial tachyarrhythmia time (AHRE time). Patients with LVEF \>50% and atrioventricular (AV) conduction disorders requiring a dual-chamber pacemaker will be randomized to either conventional RV septal pacing or LBBP.

This description comes directly from the study's public registry record.

Talk to the study team

GEORGIOS LEVENTOPOULOS  ·  +306977786020  ·  levent2669@gmail.com

Periklis Davlouros  ·  +306986726300  ·  pdav@upatras.gr

Always discuss trial participation with your own doctor first.

Locations (1)

University General Hospital of PatrasPátrai, GreeceRecruiting

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Source record: clinicaltrials.gov/study/NCT07250529