Coronary Artery Disease Clinical Trial
Official title:
Evaluate the Continued Safety and Effectiveness of the XIENCE PRIME EECSS in a Cohort of Real-world Patients Receiving the XIENCE PRIME EECSS During Commercial Use.
Abbott Vascular (AV) obtained marketing approval for the XIENCE PRIME Everolimus Eluting
Coronary Stent System (XIENCE PRIME EECSS) in China from the China Food and Drug
Administration (CFDA) on August 10th, 2011.
This prospective, observational, open-label, multi-center, single-arm, post-approval study is
designed to evaluate the continued safety and effectiveness of the XIENCE PRIME EECSS in a
cohort of real-world patients receiving the XIENCE PRIME EECSS during commercial use in
real-world settings in China.
This study has no primary outcome measure. All observations are of equal weight.
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