Atrial Fibrillation
Conditions
Keywords
atrial fibrillation, arrhythmia, AF ablation, antiarrhythmic agent, catheter ablation, pulmonary veins
Brief summary
The purpose of this study is to determine if the HIFU Pulmonary Vein Ablation System is effective in the treatment of paroxysmal Atrial Fibrillation compared to the control of best medical therapy with FDA approved antiarrhythmic drugs.
Detailed description
Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia affecting an estimated 2.2 million persons in the United States (US). In addition to being debilitating, AF has been identified as a leading risk factor for stroke. AF is often associated with structural heart disease, but a substantial number of AF patients have little or no detectable structural heart disease. A patient with AF is up to 5 times more likely to have a stroke than the general population. Recently, it has been demonstrated that for a significant portion of AF patients (80% - 95 %) the arrhythmia originates in one of the four pulmonary veins (PV's). Furthermore, it has been shown that isolation of this arrhythmia by ablation can, in the majority of patients (50-70%), eliminate or markedly reduce episodes of AF. Currently, there are a number of modalities being investigated to treat AF. They include radiofrequency, laser, thermal, cryo, microwave, and ultrasound ablation of targeted areas in the atrium and/or PVs. Comparison(s): Clinical success of High Intensity Focused Ultrasound (HIFU) Ablation for Pulmonary Vein Isolation in the treatment of Atrial Fibrillation, compared to medical therapy with anti-arrhythmic drugs (AADs).
Interventions
Anti-arrhythmic drug prescribed for treatment of atrial fibrillation
Anti-arrhythmic drug prescribed for the treatment of Atrial fibrillation
Anti-arrhythmic drug prescribed for treatment of atrial fibrillation
Anti-arrhythmic Drug prescribed for treatment of Atrial Fibrillation
Electrical isolation of pulmonary vein with high-intensity focused ultrasound
Anti-arrhythmic Drug prescribed for the treatment of Atrial Fibrillation
Sponsors
Study design
Eligibility
Inclusion criteria
* Documented atrial fibrillation * Failed or intolerant to at least 1 anti-arrhythmic drug * Able to take anti-coagulant therapy * Able to complete screening tests required for inclusion/
Exclusion criteria
* Able to take at least 1 approved anti-arrhythmic drug * Not pregnant * Available for follow-up for at least 12 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute treatment with elimination of AF episodes | 12 months |
| Death, stroke, and hospitalization for recurrence of AF | within 12 months of treatment |
Secondary
| Measure | Time frame |
|---|---|
| Acute treatment success | 60 days |
Countries
Czechia, United States