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Clinical Trial Summary

This clinical investigation is intended to demonstrate safety and effectiveness of the Volt™ Pulsed Field Ablation (PFA) Catheter Sensor Enabled™, the Volt™ PFA Generator, Agilis™ NxT Steerable Introducer Dual-Reach™, and EnSite™ X EP System EnSite™ Pulsed Field Ablation Module (for simplicity of reference this device collection will hereafter be referred to as the Volt™ PFA system) for the treatment of symptomatic, recurrent, drug-refractory paroxysmal and persistent atrial fibrillation.


Clinical Trial Description

This is a pre-market, prospective, non-randomized, multicenter clinical study to demonstrate safety and effectiveness for the treatment of symptomatic, recurrent, drug-refractory paroxysmal atrial fibrillation (PAF) and persistent atrial fibrillation (PersAF). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06223789
Study type Interventional
Source Abbott Medical Devices
Contact Jessica Arrett
Phone (+1) 612-380-8445
Email jessica.arrett@abbott.com
Status Recruiting
Phase N/A
Start date April 3, 2024
Completion date January 2026

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