Coronary Artery Disease Clinical Trial
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.
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).
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).
;
Observational Model: Cohort, Time Perspective: Prospective
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