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Clinical Trial Summary

Prospective, multi-centre, randomized, open-label, parallel comparisons to evaluate

- the incidence of bleedings (COSTA-Bleed) and

- the incidence of ischemic and bleeding events (COSTA-Outcome) following a therapy with the abluminal sirolimus coated bio-engineered stent (COMBO stent) in association with short-term single antiplatelet therapy as compared to a guidelines-based strategy in patients with coronary artery disease with an indication for chronic oral anticoagulant therapy.


Clinical Trial Description

The COSTA trials are investigator-initiated studies aimed at comparing the clinical outcome after percutaneous coronary intervention (PCI) using a COMBO-stent based strategy associated with short-term antiplatelet therapy with a guidelines-based therapy in patients with an indication for chronic oral anticoagulation. The study is organized as a national, multi-centre prospective, randomized trial. The duration of the follow-up is 15 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02723981
Study type Interventional
Source IHF GmbH - Institut für Herzinfarktforschung
Contact
Status Withdrawn
Phase Phase 4
Start date April 2016
Completion date December 2018

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