Ignite Creation Date:
2024-05-05 @ 11:43 AM
Last Modification Date:
2024-10-26 @ 9:12 AM
Study NCT ID:
NCT00111488
Status:
TERMINATED
Last Update Posted:
2016-01-06
First Post:
2005-05-20
Brief Title:
Guidant Microwave Ablation System for the Treatment of Atrial Fibrillation
Sponsor:
Boston Scientific Corporation
Organization:
Boston Scientific Corporation
Study Overview
Official Title:
Randomized Study of Surgical Ablation With Microwave Energy for the Treatment of Atrial Fibrillation
Status:
TERMINATED
Status Verified Date:
2014-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Slow enrollment
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of the Randomized Study of Surgical Ablation with Microwave Energy for the Treatment of Atrial Fibrillation RESOLVE-AF trial is to determine the safety and effectiveness of the Guidant FLEX Microwave Surgical Ablation System in the treatment of permanent atrial fibrillation AF
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None