Trials / Completed
CompletedNCT01900678
A Study of the Safety and Efficacy of the VytronUS Low-Intensity Collimated Ultrasound Ablation System
VLIC-USA: A Single-Center Study of the Safety and Efficacy of the VytronUS Low-Intensity Collimated Ultrasound Ablation System
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- VytronUS, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this investigation is to evaluate whether pulmonary vein isolation using the VytronUS ablation system is safe and effective acutely and at 3 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | VytronUS Ablation System | Pulmonary vein isolation. |
Timeline
- Start date
- 2013-06-01
- Primary completion
- 2015-01-01
- Completion
- 2015-01-01
- First posted
- 2013-07-16
- Last updated
- 2015-06-29
Locations
1 site across 1 country: Czechia
Source: ClinicalTrials.gov record NCT01900678. Inclusion in this directory is not an endorsement.