NCT01900678View on ClinicalTrials.gov

A Study of the Safety and Efficacy of the VytronUS Low-Intensity Collimated Ultrasound Ablation System

NACompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

June 30, 2013

Primary Completion Date

January 31, 2015

Study Completion Date

January 31, 2015

Conditions
Paroxysmal Atrial Fibrillation
Interventions
DEVICE

VytronUS Ablation System

Pulmonary vein isolation.

Trial Locations (1)

Unknown

Na Homolce Hospital, Prague

All Listed Sponsors
lead

VytronUS, Inc.

INDUSTRY

NCT01900678 - A Study of the Safety and Efficacy of the VytronUS Low-Intensity Collimated Ultrasound Ablation System | Biotech Hunter | Biotech Hunter