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Clinical Trial Summary

The primary objective of this study is to compare two different regimens of therapy, AVK and ASA (aspirin), in the early postoperative period after aortic valve replacement with SJM Epic™ or SJM Epic™ Supra Porcine Bioprosthetic Heart Valve by establishing the adverse event free survival rate at 3 month post intervention follow-up of the 2 groups(with special focus on thromboembolic events and bleedings).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00187304
Study type Interventional
Source Abbott Medical Devices
Contact
Status Withdrawn
Phase Phase 4
Start date September 2005

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