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Study identifier: NCT07236489 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Trial Evaluating the Benefit of Left Bundle Branch Area Stimulation Compared With Conventional Pacing in Post-TAVI Atrioventricular Atrioventricular Block

Condition: Atrioventricular Block · Pacemaker  ·  Sponsor: Nantes University Hospital

PhaseNA
Planned participants266
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Transcatheter aortic valve implantation (TAVI) has rapidly expanded over the past decade as a treatment for severe aortic valve stenosis, with over 14,000 procedures performed in France in 2021. A common complication following TAVI is traumatic atrioventricular block requiring pacemaker implantation, occurring in about 10% of patients. Conventional right ventricular pacing in these cases often leads to interventricular dyssynchrony, which can impair left ventricular ejection fraction and increase the risk of hospitalization, heart failure, and mortality. Cardiac resynchronization therapy via biventricular pacing is sometimes proposed as a secondary intervention but involves additional surgery. A newer pacing technique-selective left bundle branch area pacing-has been developed to provide physiological ventricular activation by stimulating conduction pathways distal to the lesion, thereby avoiding dyssynchrony. Retrospective studies suggest clinical benefits, but no prospective randomized trial has yet evaluated its efficacy compared to standard pacing. The objective of this study is to conduct the first randomized clinical trial comparing left bundle branch area pacing versus conventional right ventricular pacing in patients requiring pacemaker implantation due to atrioventricular block after TAVI.

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

Talk to the study team

Research and Innovation Departement of Nantes UH  ·  +33253482810  ·  bp-prom-regl@chu-nantes.fr

Damien MINOIS, M.D  ·  +33244768742  ·  damien.minois@chu-nantes.fr

Always discuss trial participation with your own doctor first.

Locations (7)

Brest University HospitalBrest, Finistère, FranceRecruiting
Rennes University HospitalRennes, Ille-et-Vilaine, FranceRecruiting
Tours University HospitalTours, Indre-et-Loire, FranceRecruiting
Nantes University HospitalNantes, Loire-Atlantique, FranceRecruiting
Clermont Ferrand University HospitalClermont-Ferrand, Puy-de-Dôme, FranceNot Yet Recruiting
Rouen University HospitalRouen, Seine-Maritime, FranceRecruiting
Poitiers University HospitalPoitiers, Vienne, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07236489