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Clinical Trial Summary

The study will enroll patients with angiographically significant coronary de novo lesions. Subjects will be randomized 1:1 and treated with a Lutonix catheter either before or after bare-metal stenting (BMS). The purpose is to assess the feasibility, safety and efficacy of the Lutonix Catheter for treatment of de novo coronary artery stenosis using two distinct treatment strategies.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00934752
Study type Interventional
Source C. R. Bard
Contact
Status Completed
Phase Phase 1/Phase 2
Start date July 2009
Completion date January 2012

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