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Clinical Trial Summary

The purpose of this study is to determine whether patients undergoing coronary intervention that also require oral anticoagulation, treatment with the COBRA PzF stent plus 14-day dual anti-platelet therapy (DAPT) has higher safety and non-inferior outcomes for thrombo-embolic events than compared with standard FDA-approved drug eluting stent (DES) plus 3 or 6-month DAPT.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02594501
Study type Interventional
Source CeloNova BioSciences, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date February 5, 2016
Completion date November 2021

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