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Comparing two heart pacing methods in people with atrial fibrillation and weak heart pumping

Compares two heart pacing methods in adults with atrial fibrillation and weakened heart function.

Plain-language title generated from the registry record
Registry title: Left Bundle Branch Area Pacing or Biventricular Pacing in AF and Left Ventricular Dysfunction

Key facts

Where
Aarhus N, DenmarkSee the site

Where in Denmark

  • Aarhus University HospitalAarhus N, DenmarkNot yet recruiting

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Trial details

Who runs it
srdpiers
Trial code
NCT06620705
Record updated
1 October 2024
Original description
It is unknown whether left bundle branch area pacing (LBBAP) or biventricular pacing best prevents or reverses left ventricular (LV) adverse remodelling in patients with atrial fibrillation (AF) who require ventricular pacing or CRT. This randomized non-inferiority cross-over trial will compare left ventricular end-systolic volume change and secondary endpoints between LBBAP and biventricular pacing in patients with AF and LV dysfunction.Read full original descriptionShow less

Pacing Away from Heart Failure: Left Bundle Branch Area Pacing or Biventricular Pacing in Patients with Atrial Fibrillation and Left Ventricular Dysfunction

It is unknown whether left bundle branch area pacing (LBBAP) or biventricular pacing best prevents or reverses left ventricular (LV) adverse remodelling in patients with atrial fibrillation (AF) who require ventricular pacing or CRT. This randomized non-inferiority cross-over trial will compare left ventricular end-systolic volume change and secondary endpoints between LBBAP and biventricular pacing in patients with AF and LV dysfunction.

Inclusion: In order to be eligible to participate in this study, a subject must meet all of the following criteria:; Adults ≥18 years with permanent AF and LVEF \< 50% who either require ventricular pacing because of bradycardia including patients undergoing AV junction ablation, or have an indication for cardiac resynchronization therapy; Expected percentage of ventricular pacing \> 40%; ≥ 3 months of heart failure medication optimization; Of note, patients who already have a device, but require an upgrade to a CRT device, can also be included.

Exclusion: Recent valve intervention/surgery or acute myocardial infarction (\< 6 months); NYHA functional class IV heart failure, left ventricular assist device or cardiac transplant; Age \< 18 years; A potential subject who meets any of the following criteria will be excluded from participation in this study:; Pregnancy or active pregnancy wish; Not eligible for implantation of an RV lead, LBBAP lead, or LV lead in the coronary sinus.

ClinicalTrials.gov NCT06620705