Trials / Terminated
TerminatedNCT01103661
Safety and Efficacy Study of The Combined Ablation Procedure To Treat Longstanding Persistent Atrial Fibrillation
Feasibility Study For Safety and Efficacy Evaluation Of The Combined Ablation Procedure For The Treatment Of LongStanding Persistent Atrial Fibrillation
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- nContact Surgical Inc. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This is a multi-center, prospective open label, feasibility study evaluating the safety and efficacy of the combined ablation procedure for the treatment of longstanding persistent atrial fibrillation.
Detailed description
The purpose of this feasibility study is to evaluate the safety and efficacy of the epicardial / endocardial combined procedure using the nContact Numeris®-AF Guided Coagulation System with VisiTrax® epicardially and the St. Jude Medical Therapy™ Cool Path™ Ablation Catheter endocardially to treat longstanding persistent Atrial Fibrillation (AF) patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Numeris®-AF Guided Coagulation System with VisiTrax® | Combined epicardial / endocardial procedure using the nContact Numeris®-AF Guided Coagulation System with VisiTrax® epicardially and the St. Jude Medical Therapy™ Cool Path™ Ablation Catheter endocardially. |
Timeline
- Start date
- 2010-04-01
- Primary completion
- 2012-10-01
- Completion
- 2013-04-01
- First posted
- 2010-04-15
- Last updated
- 2014-04-03
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01103661. Inclusion in this directory is not an endorsement.