Ignite Creation Date:
2024-05-05 @ 9:44 PM
Last Modification Date:
2024-10-26 @ 10:09 AM
Study NCT ID:
NCT00958165
Status:
COMPLETED
Last Update Posted:
2016-08-30
First Post:
2009-08-12
Brief Title:
Clinical Study of the CardioFocus Endoscopic Ablation System for the Treatment of Symptomatic AF
Sponsor:
CardioFocus
Organization:
CardioFocus
Study Overview
Official Title:
Clinical Study of the CardioFocus Endoscopic Ablation System - Adaptive Contact CFEAS- AC for the Treatment of Symptomatic Atrial Fibrillation
Status:
COMPLETED
Status Verified Date:
2016-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to determine the safety and effectiveness of the endoscopic ablation system - adaptive contact EAS-AC in treated paroxysmal atrial fibrillation PAF with pulmonary vein isolation PVI
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