XIENCE PRIME Japan Post-Marketing Surveillance (PMS)

Status Completed

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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