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The objective of the study is to evaluate the safety and efficacy of XIENCE PRIME SV in real world practice in Japanese hospitals.
Based on Good Post-marketing Study Practice (GPSP) regulation, general patient population with ischemic heart disease who are eligible for treatment with XIENCE PRIME SV Everolimus Eluting Stent will be registered, with no particular inclusion/exclusion criteria, and may be eligible for angiographic follow-up at eight months and clinical follow-up at one year.
Observational Model: Cohort, Time Perspective: Prospective
Ischemic Heart Disease
XIENCE PRIME SV Everolimus Eluting Coronary Stent
Kimitsu Chuo Hospital
Active, not recruiting
Published on BioPortfolio: 2015-08-03T15:53:24-0400
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