VOLT-AF IDE Clinical Study

Status Recruiting

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

Clinical Trial Details

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

View Details

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