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Clinical Trial Summary

The primary objective of the LEVANT 2 Extended Follow-up Post-Approval Study (PAS 1) is to evaluate the long-term performance of the Lutonix Drug Coated Balloon (DCB) versus Percutaneous Transluminal Balloon Angioplasty (PTA) in the treatment of stenosis or occlusion of the femoropopliteal arteries.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01790243
Study type Interventional
Source C. R. Bard
Contact
Status Completed
Phase N/A
Start date July 20, 2011
Completion date November 1, 2018

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