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Assessment of the Effect of Catheter Ablation on Elderly Population With Atrial Fibrillation; a Randomized Controlled Study; The ACE-AF Study

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Procedure, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

ACE-AF is a multicenter randomized study in people aged 78 years and older with symptomatic atrial fibrillation (AF). AF is a common heart rhythm disorder in older adults and can cause reduced quality of life and lead to serious complications such as stroke and heart failure. The study compares two established treatment strategies: 1. Catheter ablation (an invasive procedure aimed at reducing AF by electrically isolating triggers in the heart, primarily through pulmonary vein isolation), and 2. Optimized medical therapy without AF ablation (medications for rate and/or rhythm control; AV node ablation with pacemaker may be used if clinically indicated according to routine care). Participants are randomized 1:1 to one of these strategies. All participants will receive an implantable loop recorder (a small heart rhythm monitor placed under the skin) to continuously track heart rhythm and measure AF burden over time. The study has two primary endpoints, tested with Holm-Bonferroni multiplicity control assessed over 24 months: 1. a composite of major clinical events (all-cause mortality, stroke, major bleeding, cardiac arrest, or hospitalization due to heart failure), and 2. patient-reported health-related quality of life (HRQoL), measured by the RAND-36 General Health domain. ACE-AF will provide evidence to guide treatment decisions for very elderly patients with symptomatic AF and help identify which patients benefit most from an ablation-based strategy compared with optimized medical therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 78
Healthy Volunteers: f
View:

• Age ≥78 years.

• ECG-documented atrial fibrillation.

• AF type: paroxysmal, persistent, or longstanding persistent AF.

• Suitable candidate for catheter ablation according to ESC guidelines.

• Charlson's comorbidity index ≤7.

Locations
Other Locations
Sweden
Linköping University Hospital
NOT_YET_RECRUITING
Linköping
Karolinska University Hospital
RECRUITING
Stockholm
Contact Information
Primary
Emmanouil Charitakis, MD, PhD
emmanouil.charitakis@regionstockholm.se
0046767877506
Backup
Nikola Drca, MD, PhD
emmanouil.charitakis@regionstockholm.se
+46705949838
Time Frame
Start Date: 2026-10-05
Estimated Completion Date: 2034-09-15
Participants
Target number of participants: 282
Treatments
Active_comparator: Catheter Ablation Strategy
Participants randomized to this arm will undergo catheter ablation for atrial fibrillation, with pulmonary vein isolation (PVI) prioritized as the primary ablation strategy. Energy source and tools are selected according to local practice and operator discretion (no restriction to a specific technology). Participants will also receive an implantable loop recorder (ILR) for continuous rhythm monitoring throughout follow-up. Additional medical therapy may be used as clinically indicated according to guideline-based care.
Active_comparator: Optimized Medical Therapy (Rate/Rhythm control) ± AV Node Ablation + Pacing
Participants randomized to this arm will receive optimized guideline-directed medical therapy for atrial fibrillation without AF catheter ablation. Treatment may include rate control and/or rhythm control (including antiarrhythmic drugs and/or cardioversion when clinically appropriate). AV node ablation with pacemaker implantation is permitted when clinically indicated according to routine care. Participants will also receive an implantable loop recorder (ILR) for continuous rhythm monitoring throughout follow-up.
Sponsors
Collaborators: Royal Adelaide Hospital, University Hospital, Umeå, University Hospital, Linkoeping, Lund University Hospital, Uppsala University Hospital, Onassis Cardiac Surgery Centre, Sahlgrenska University Hospital, Dept of Cardiology, Örebro University Hospital, Sweden
Leads: Karolinska University Hospital

This content was sourced from clinicaltrials.gov