A clinical and angiographic study of the XIENCE V everolimus-eluting coronary stent system in the treatment of patients with multivessel coronary artery disease: the EXECUTIVE trial (EXecutive RCT: evaluating XIENCE V in a multi vessel disease).

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Summary

The study shows lower in-stent late loss at 9 months with the EES XIENCE V compared with the PES TAXUS Libertè, and a low major adverse cardiac event rate at 1 year in patients with 2- to 3-vessel MV-CAD.

Type
article
Published
2013-10-01
Cited by
31
References
37
Access
Open access

Keywords

Medicine, Clinical endpoint, Coronary artery disease, Stent, Myocardial infarction

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