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Product Surveillance Registry — PSR  

Coronary Artery Disease Clinical Trial

Official title:
Medtronic Product Surveillance Registry

Clinical Trial Summary

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01524276
Study type Observational
Source Medtronic
Contact Medtronic Product Surveillance Registry
Email rs.productsurveillanceregistry@medtronic.com
Status Recruiting
Phase
Start date January 2012
Completion date January 2030
View Details
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