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Clinical Trial Summary

The propose of this study is to demonstrate, whenever using Drug Eluting Stent is not possible, the clinical security at 12 months, of the combinaison Bare Metal Stent plus Drug Eluting Balloon.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01930903
Study type Interventional
Source Biotronik France
Contact
Status Active, not recruiting
Phase N/A
Start date September 2013
Completion date December 2015

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