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| Name | Class |
|---|---|
| Medtronic France SAS | INDUSTRY |
| ClinSearch | OTHER |
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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 :
Heart failure with preserved ejection fraction is a major public health issue affecting 4.9% of general population aged ≥ 60 years. It accounts for more than half of all heart failure hospital admissions. Atrial fibrillation is very common in this diseased population as pathophysiologies are highly interrelated. Atrial fibrillation occurs in two thirds of Heart failure with preserved ejection patients at some point in the natural history and confers a poor prognosis. Therapeutic alternatives are currently limited as patients with permanent Atrial fibrillation and Heart failure with preserved ejection are often treated with drug therapies for lenient rate control.
Recently, the APAF-CRT mortality trial demonstrated a reduction in mortality and hospitalization in Heart Failure and Atrial fibrillation patients treated with Atrioventricular node ablation plus Cardiac Resynchronization Therapy versus pharmacological rate control, irrespective of their baseline Ejection Fraction. The optimal rate regularization achieved with atrioventricular node ablation emerges as the main determinant of reduction in mortality and hospitalization. This conclusion is supported by old robust physiology studies showing that beat-to-beat heart rate irregularity has significant hemodynamic effects and notably decreases cardiac output. However, no specific trials have been conducted in patients with Heart failure with preserved ejection, a population for whom treatment strategies that effectively improve outcomes are sparse. We aim at analyzing the benefit of heart rate regularization and physiological pacing in patients with Heart failure with preserved ejection (Left Ventricular Ejection Fraction ≥ 50%) and permanent Atrial Fibrilation.
We hypothesize that heart rate regularization added to physiological pacing - preventing the deleterious effect of right ventricular apical pacing - would reduce mortality and Heart Failure hospitalizations.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention group with pacemaker implantation and atrioventricular node ablation | Experimental | Pacemaker implantation and atrioventricular node ablation will be performed within a one week period after the randomization.Pharmacological heart failure therapy will be optimized according to current guidelines. |
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| Control | No Intervention | Conventional care support. The rate control therapy will be optimized to achieve a resting heart rate of <110 beats per minute. Pharmacological heart failure therapy will be optimized according to current guidelines. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| pacemaker implantation | Procedure | The Medtronic 3830 lead should be used as the Conduction System Pacing lead. However, in case of unsuccessful implantation with the 3830 lead, a stylet-driven lead can be used as an alternative. |
| Measure | Description | Time Frame |
|---|---|---|
| Time to the composite of all-cause mortality or hospitalization due to heart failure or intravenous diuretics. | Delay between randomization and death or hospitalization or intravenous diuretics due to heart failure | 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| Time to all-cause mortality | Delay between randomization and death (all-cause). | 24 months |
| Time to Cardiovascular mortality | Delay between randomization and death due to cardiovascular disease. |
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Inclusion Criteria:
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
Presence of at least one of the following criteria related to diastolic dysfunction:
Narrow QRS ≤ 120 ms
Average heart rate ≤ 110/min on 24 hours Holter monitoring
Age over 18-year-old
Capacity to understand the nature of the study, legal ability and willingness to give informed consent
Patient covered by a social insurance
Effective contraception and a negative pregnancy test in women of a childbearing age
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Tessa BERGOT, MSc | Contact | +33144907033 | tessa.bergot@sfcardio.fr |
| Name | Affiliation | Role |
|---|---|---|
| Frédéric ANSELME, MD | CHU de Rouen, France | Principal Investigator |
| Corentin CHAUMONT, MD | CHU de Rouen, France | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| OLV Aalst | Not yet recruiting | Aalst | 9300 | Belgium |
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Randomization 1:1 Intervention arm: Conduction system pacing (pacemaker implantation) + atrioventricular node ablation Control arm: optimal pharmacological therapy
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Clinical outcomes will be adjudicated by the investigator and reviewed by the Clinical Events Committee, which will be blinded to treatment received by the patient.
| atrioventricular node ablation | Procedure | Right-sided atrioventricular junction ablation will be attempted first with a radiofrequency catheter. The choice of the catheter will be at the discretion of the physician. The catheter will be advanced to the His Bundle and then slightly withdrawn proximally and caudally in order to target the compact atrioventricular node. Repeated ablation procedures will be recommended during follow-up if regression of atrioventricular block occurs. |
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| Pacemaker programming | Device | The pacemaker device will be programmed in VVIR mode at a lower rate of 75 beats per minute in bipolar mode for sensing and pacing |
|
| 24 months |
| Time to heart failure hospitalization | Delay between randomization and hospitalization due to heart failure. | 24 months |
| Change in New York Heart Association score | Evolution of the functional status measured by New York Heart Association score between randomization and 24 months follow up visit. From II (mild), III (moderate) to IV (severe). | 24 months |
| Change in B-type natriuretic peptide level | Evolution of B-type natriuretic peptide (BNP) level between randomization and 24 months follow up visit. | 24 months |
| Major adverse events following pacemaker implantation | Record of safety information about pacemaker implantation procedure | 24 months |
| Major adverse events following atrioventricular node ablation | Record of safety information about atrioventricular node ablation procedure | 24 months |
| UZ Leuven | Not yet recruiting | Leuven | 3000 | Belgium |
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| Clinique St Pierre Ottignies | Not yet recruiting | Ottignies-Louvain-la-Neuve | 1340 | Belgium |
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| CHRU de Brest - Hôpital de la Cavale Blanche | Not yet recruiting | Brest | 29200 | France |
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| CHRU de Caen | Not yet recruiting | Caen | 14000 | France |
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| CHRU de Tours - Trousseau | Not yet recruiting | Chambray-lès-Tours | 37170 | France |
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| CHU Grenoble Alpes | Not yet recruiting | Grenoble | 38043 | France |
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| Groupe Hospitalier La Rochelle-Ré-Aunis | Not yet recruiting | La Rochelle | 17019 | France |
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| CHRU Lille | Not yet recruiting | Lille | 59000 | France |
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| GHICL Allome - Hôpital St Philibert | Not yet recruiting | Lomme | 59462 | France |
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| Clinique Millenaire | Not yet recruiting | Montpellier | 34000 | France |
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| CHU de Nantes - Hôpital Nord Laennec | Not yet recruiting | Nantes | 44093 | France |
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| CHU de Bordeaux - Hôpital Cardiologique du Haut-Lévèque | Not yet recruiting | Pessac | 33604 | France |
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| CHU Poitiers | Recruiting | Poitiers | 86021 | France |
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| CHU de Rouen | Not yet recruiting | Rouen | 76000 | France |
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| ID | Term |
|---|---|
| D001281 | Atrial Fibrillation |
| D006333 | Heart Failure |
| ID | Term |
|---|---|
| D001145 | Arrhythmias, Cardiac |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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