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

Coronary Artery Disease Clinical Trial

Official title:
XIENCE Xpedition 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 Xpedition Everolimus-Eluting 2.25mm Stent 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 Xpedition Everolimus-Eluting 2.25mm 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. The XIENCE Xpedition 2.25 mm stent is composed of the stent identical to the stent of the XIENCE PRIME SV Stent.Therefore, the data collected from the PMS will be pooled with data collected from the ongoing XIENCE PRIME SV PMS for analysis. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02513732
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date July 2014
Completion date September 2020
View Details
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