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RECRUITING Not applicable ClinicalTrials.gov

Catheter Ablation vs Conservative Care in Elderly Patients With Atrial Fibrillation

Sponsor: Karolinska University Hospital • ClinicalTrials.gov ID: NCT07424690

Registry updated: 2026-10-08
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Description

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.

Interventions

  • Catheter Ablation for Atrial Fibrillation (Procedure)
    Catheter ablation for symptomatic atrial fibrillation with pulmonary vein isolation (PVI) prioritized as the primary lesion set. Energy source and tools are selected according to local practice and operator discretion (no restriction to a specific technology), performed under routine standards of care at experienced centres.
  • Optimized Medical Therapy for Atrial Fibrillation (Drug)
    Guideline-directed rate and/or rhythm control tailored to the participant's clinical condition, including rate-control medications and/or antiarrhythmic drugs and cardioversion when clinically appropriate. AF ablation is not performed as part of this strategy.
  • Implantable Loop Recorder (ILR) (Device)
    Subcutaneous implantable loop recorder used for continuous rhythm monitoring and quantification of atrial fibrillation burden throughout follow-up. Implanted in all participants according to protocol-defined workflow.
  • AV Node Ablation With Pacemaker implantation (Procedure)
    AV node ablation with permanent pacing may be performed when clinically indicated according to routine care, as part of the optimized medical therapy strategy.

Eligibility criteria

Inclusion Criteria: 1. Age ≥78 years. 2. ECG-documented atrial fibrillation. 3. AF type: paroxysmal, persistent, or longstanding persistent AF. 4. Suitable candidate for catheter ablation according to ESC guidelines. 5. Charlson's comorbidity index ≤7. Exclusion Criteria: 1. Left atrial (LA) dimension \>55 mm, based on echocardiography within the previous year. 2. Acute coronary syndrome or coronary artery bypass surgery within the last 12 weeks. 3. Severe valvular heart disease (per ESC definitions) or congenital heart disease. 4. Prior surgical or catheter AF ablation procedure, or prior AV-node (atrioventricular nodal) ablation. 5. Contraindication to oral anticoagulation. 6. AF due to a reversible cause. 7. Medical condition likely to limit survival to \<12 months. 8. Unable or unwilling to provide informed consent. 9. History of non-compliance with medical therapy. 10. BMI \<18 or \>37 kg/m².

Conditions

Atrial Fibrillation (AF) Atrial Fibrillation Ablation Elderly

Locations

  • Linköping University Hospital — Linköping, Sweden
  • Karolinska University Hospital — Stockholm, Sweden
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record