Atrial Fibrillation Clinical Trial
Official title:
Atrial Fibrillation Ablation Pilot Study- Study Number AFI-20
This is a prospective, non-randomized, multicenter, multi-country pilot study to evaluate the safety and effectiveness of the Ablation Frontiers Cardiac Ablation System for the ablative treatment of symptomatic permanent atrial fibrillation.
The study shall be conducted according to ISO 14155. Results of this research study will be
used to assess the performance and safety of the System and its components. Data may be
combined with similar research at additional sites to create a greater understanding of the
endpoints. Up to sixty (60) patients (including "roll-in" or training patients) will be
enrolled in a non-randomized study to assess the safety and efficacy of the Ablation
Frontiers Cardiac Ablation System. Further studies may be performed to gather additional data
regarding the safety and efficacy of the system.
Patients with a history of symptomatic permanent AF, willing and able to sign an informed
consent, and meeting all inclusion/exclusion criteria, as identified by the clinical
investigator, will be enrolled in the study. Comparative and descriptive statistics will be
used to summarize patient outcomes for the specified study endpoints.
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