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Clinical Trial Summary

To assess strut coverage in patients presenting an acute myocardial infarction and treated either with the SYNERGY stent or the Bioresorbable Vascular Scaffold, through a parallel group design.


Clinical Trial Description

Single center, simple-blind randomized controlled trial, comparing the SYNERGY stent with the BVS device through a parallel group design. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02890589
Study type Interventional
Source University Hospital, Toulouse
Contact
Status Completed
Phase N/A
Start date July 2016
Completion date February 2018

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