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Clinical Trial Summary

The purpose of this study is: To evaluate the safety and performance of the Presillion stent in routine clinical practice.


Clinical Trial Description

Primary endpoint: Composite of Major Adverse Cardiac Events (MACE), which includes cardiac death, myocardial infarction (Q-wave and non Q-wave) and clinically driven target lesion revascularization (TLR) at 12 months follow-up.

Data will be collected on 400 patients (from 14 hospitals in Spain and Portugal) treated with the Presillion stent in up to 2 de novo native coronary artery lesions

Study design: multicenter, prospective, observational ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00968019
Study type Observational
Source Johnson and Johnson, S.A.
Contact
Status Completed
Phase N/A
Start date April 2009
Completion date May 2011

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