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XIENCE PRIME Japan Post-Marketing Surveillance (PMS)

Coronary Artery Disease Clinical Trial

Official title:
XIENCE PRIME Everolimus Eluting Coronary Stent Post Marketing Surveillance (PMS) in Japan

Clinical Trial Summary

The objectives of the PMS are to observe the frequency, type, and degree of device deficiency to assure the safety of the new medical device (XIENCE PRIME) as well as to collect information on evaluation of the efficacy and safety for reevaluation.

Clinical Trial Description

The primary objectives of the PMS are to observe the frequency, type, and degree of device deficiency to assure the safety of the new medical device (XIENCE PRIME) as well as to collect information on evaluation of the efficacy and safety for reevaluation by Pharmaceuticals and Medical Devices Agency (PMDA). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01721096
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date October 2012
Completion date November 2018
View Details
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