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XIENCE V/PROMUS Everolimus-Eluting Stent System Post-marketing Surveillance Protocol for Japan

Coronary Artery Disease Clinical Trial

Official title:
XIENCE V/PROMUS Everolimus-Eluting Stent System Japan Post-marketing Surveillance Protocol

Clinical Trial Summary

The objectives of this post-marketing surveillance, conducted in Japan, is to know the frequency, type and degree of device malfunction, to assure the safety of the medical device, and to collect information on evaluation of the efficacy and safety.

Clinical Trial Description

The surveillance is to be conducted in accordance with the Japanese Ministerial Ordinance concerning the Standards for Postmarketing Surveillance and Tests of Medical Devices. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01086228
Study type Observational
Source Abbott Vascular
Contact
Status Completed
Phase N/A
Start date March 2010
Completion date August 2016
View Details
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