Ignite Creation Date:
2024-05-05 @ 11:21 PM
Last Modification Date:
2024-10-26 @ 10:32 AM
Study NCT ID:
NCT01310309
Status:
COMPLETED
Last Update Posted:
2012-12-21
First Post:
2011-03-03
Brief Title:
EXecutive Registry Evaluating XIENCE V in a Multi Vessel Disease
Sponsor:
Abbott Medical Devices
Organization:
Abbott Medical Devices
Study Overview
Official Title:
EXecutive Registry XIENCE V Everolimus Eluting Coronary Stent System XIENCE V EECSS in the Treatment of the Specific Setting of Patients With Multi-vessel Coronary Artery Disease
Status:
COMPLETED
Status Verified Date:
2012-12
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:
EXecutive
Brief Summary:
The purpose of this two part study is the assessment of the performance of the XIENCE V Everolimus Eluting Coronary Stent System XIENCE V EECSS in the treatment of the specific setting of patients with Multi-Vessel Coronary Artery Disease MVD
Detailed Description:
This is a clinical evaluation of the XIENCE V everolimus eluting coronary stent system as a revascularization treatment of patients with multi-vessel coronary artery disease MVD-CAD
The sutdy is composed of two parts
A Randomized Controlled Trial outlined in a separate posting and the registry portion of this study which is as follows
-A prospective controlled registry to analyze the clinical efficacy and safety at mid and long-term follow-up in patients with MVD treated with the XIENCE V Everolimus Eluting Coronary Stent System XIENCE V EECSS
The sutdy is composed of two parts
A Randomized Controlled Trial outlined in a separate posting and the registry portion of this study which is as follows
-A prospective controlled registry to analyze the clinical efficacy and safety at mid and long-term follow-up in patients with MVD treated with the XIENCE V Everolimus Eluting Coronary Stent System XIENCE V EECSS
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