Trials / Terminated
TerminatedNCT00950092
nContactSurgical Numeris-AF Tethered Coagulation System for Treatment of Persistent & LSP AF
Numeris-AF Tethered Coagulation System With VisiTrax Indicated For Treatment of Persistent and Longstanding Persistent Atrial Fibrillation
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 5 (actual)
- Sponsor
- nContact Surgical Inc. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This is a multi center, non-randomized, prospective, open label, clinical trial evaluating the safety and efficacy of the nContact Surgical Numeris-AF Tethered Coagulation System when used to treat patients with persistent and longstanding persistent AF during concomitant cardiac surgery.
Detailed description
The purpose of this study is to determine the safety and efficacy of the Numeris-AF Tethered Coagulation System with VisiTrax when used to treat persistent and longstanding persistent Atrial Fibrillation(AF)during concomitant cardiac surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Numeris-AF Tethered Coagulation System with VisiTrax | Surgical radiofrequency (RF) epicardial ablation using the nContact Numeris-AF Tethered Coagulation System |
Timeline
- Start date
- 2009-10-01
- Primary completion
- 2013-06-01
- Completion
- 2013-10-01
- First posted
- 2009-07-31
- Last updated
- 2014-04-03
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00950092. Inclusion in this directory is not an endorsement.