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Study identifier: NCT06436053 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Acute Response to Left Bundle Branch Area Pacing With SyncAV

Condition: Heart Failure  ·  Sponsor: Abbott Medical Devices

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This clinical investigation is a prospective, single-arm, post-market, non-randomized, single-center study designed to evaluate the effectiveness of the SyncAV CRT dynamic atrioventricular (AV) delay feature when used with left bundle branch area pacing (LBBAP).

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

Talk to the study team

Nima Badie, PhD  ·  408-702-8604  ·  nima.badie@abbott.com

Always discuss trial participation with your own doctor first.

Locations (1)

I.R.C.C.S. Policlinico San DonatoSan Donato Milanese, MI, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06436053