About this trial
The goal of this clinical trial is to assess the clinical efficacy of physiological pacing combined with atrioventricular node ablation, in patients with Heart Failure with preserved Ejection Fraction (HFpEF) and well controlled permanent atrial fibrillation.The main question it aims to answer is that heart rate regularization added to physiological pacing - preventing the deleterious effect of right ventricular apical pacing - would reduce mortality and heart failure hospitalizations.
Researchers will compare physiological pacing combined with atrioventricular node ablation (intervention arm) versus optimal pharmacological therapy (control arm) to see if physiological pacing combined with atrioventricular node ablation reduce time to the composite of all-cause mortality or hospitalization due to heart failure or intravenous diuretics (time frame 24 months).
Participants will :
* Be randomized in intervention arm or control arm. * Visit the clinic 3 months, 12 months and 24 months after the randomization for checkups and tests.
Eligibility criteria
Qualifiers
Permanent atrial fibrilation > 6 months
Preserved Left Ventricular Ejection Fraction ≥ 50%
≥ 1 heart failure hospitalization in the previous year
NYHA (New York Heart Association) score ≥ 2
Disqualifiers
Patient eligible for atrial fibrilation catheter ablation
Life expectancy < 12 months
Severe chronic kidney disease (estimated Glomerular Filtration Rate ≤ 20 ml/1,73 m2)
Severe respiratory disease (severe chronic obstructive pulmonary disease with Gold ≥ 3 and/or chronic oxygen therapy)
Trial design
Treatments tested in this trial
- pacemaker implantation
- atrioventricular node ablation
- Pacemaker programming