Ignite Creation Date:
2024-05-05 @ 11:42 AM
Last Modification Date:
2024-10-26 @ 9:12 AM
Study NCT ID:
NCT00116428
Status:
COMPLETED
Last Update Posted:
2017-10-24
First Post:
2005-06-29
Brief Title:
NAVISTAR THERMOCOOL Catheter for the Radiofrequency Ablation of Symptomatic Paroxysmal Atrial Fibrillation
Sponsor:
Biosense Webster Inc
Organization:
Biosense Webster Inc
Study Overview
Official Title:
NAVISTAR THERMOCOOL Catheter for the Radiofrequency Ablation of Symptomatic Paroxysmal Atrial Fibrillation
Status:
COMPLETED
Status Verified Date:
2017-09
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:
Afib IDE
Brief Summary:
This trial compares the safety and effectiveness of catheter ablation for PAF with antiarrhythmic drug therapy The investigational catheter being studied is the NAVISTAR THERMOCOOL irrigated-tip catheter At the time of this study the NAVISTAR THERMOCOOL catheter was FDA-approved for commercial distribution in the US for treating patients with Type I atrial flutter and drug refractory monomorphic ventricular tachycardia post myocardial infarction The catheter was approved for use in Europe for endocardial ablation for treating cardiac arrhythmias
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