Trials / Terminated
TerminatedNCT00741611
Study of HD Mesh Ablation System for Treatment of Paroxysmal Atrial Fibrillation
A Randomized Controlled Trial of Radiofrequency Ablation for the Treatment of Paroxysmal Atrial Fibrillation Using the Bard High Density Mesh Ablation System (MAGELLAN)
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 44 (actual)
- Sponsor
- C. R. Bard · Industry
- Sex
- All
- Age
- 21 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This is a randomized controlled study of the Bard High Density Mesh Ablation System for treatment of paroxysmal atrial fibrillation. This study will determine if the HD Mesh Ablation System is as safe as and more effective than anti-arrhythmic drugs.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | HD Mesh Ablation System | Ablation using the HD Mesh Ablation System |
| DRUG | Anti-arrhythmic drugs | 5 anti-arrhythmic drugs administered at the labeled dosage for atrial fibrillation |
Timeline
- Start date
- 2008-07-01
- Primary completion
- 2009-11-01
- Completion
- 2009-11-01
- First posted
- 2008-08-26
- Last updated
- 2012-10-26
- Results posted
- 2012-10-26
Locations
13 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00741611. Inclusion in this directory is not an endorsement.