VOLT CE Mark Study
NCT: NCT06106594 · ACTIVE_NOT_RECRUITING
Brief 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.
Frequently Asked Questions
What is VOLT CE Mark Study?
VOLT CE Mark Study is a clinical trial registered under NCT06106594. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT06106594?
The current status of NCT06106594 (VOLT CE Mark Study) is: ACTIVE_NOT_RECRUITING.
When did VOLT CE Mark Study start?
VOLT CE Mark Study started on 2023-10-24.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.