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Clinical Trial Summary

This is a control registry to the E-FIRM registry to track conventional atrial fibrillation (AF) procedures in terms of clinical usage, handling, and the safety and effectiveness for the treatment of symptomatic atrial fibrillation. Conventional AF ablation is defined as pulmonary vein isolation (PVI) and any additional ablation for AF according to the standard routine of the center.

Data items will be collected, if available, consistent and applicable with routine and standard clinical care at each participating site.


Clinical Trial Description

Prospective and retrospective enrollment possible ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02407249
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date April 2015
Completion date July 31, 2018

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