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XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveillance (XIENCE PRIME SV Japan PMS)

Coronary Artery Disease Clinical Trial

Official title:
XIENCE PRIME SV Everolimus Eluting Coronary Stent Japan Post Marketing Surveillance

Clinical Trial Summary

The objective of the study is to evaluate the safety and efficacy of XIENCE PRIME SV in real world practice in Japanese hospitals.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02513719
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date May 13, 2013
Completion date September 2019
View Details
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