Last updated on September 2018

Cryo AF Global Registry

Brief description of study

Cryo AF Global Registry a prospective, global, multi-center, observational Post-Market Registry

Detailed Study Description

The Cryo AF Global Registry is a prospective, global, multi-center, observational post-market registry (PMR). The purpose of this study is to evaluate and describe clinical performance and safety data in a broad patient population treated with a commercially available Arctic Front Family of Cardiac Cryoablation Catheters (hereafter referred to as "Arctic Front Cardiac Cryoablation Catheter System"). The cryoballoon ablation(CBA) procedure will be performed according to routine hospital practice. The study is expected to have a 24 month enrollment period. The follow up period is intended to align with standard practice and subjects will be followed for a minimum of 12 months post-procedure.

Clinical Study Identifier: NCT02752737

Contact Investigators or Research Sites near you

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Neuzil Petr, Prof.

Nemocnice Na Homolce
Prague, Czechia
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