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Clinical Trial Summary

A study evaluating the safety and efficacy of the BioFreedom™ Biolimus A9™ coated Cobalt Chromium coronary stent system in patients at high risk of bleeding


Clinical Trial Description

Prospective, multi-center, open-label single-arm study designed to enroll 370 HBR patients (for at least 340 evaluable) at up to 20 centers in up to 2 European countries. 370 patients will receive a BioFreedomTM CoCr stent. All patients will be followed up for 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03118895
Study type Interventional
Source Biosensors Europe SA
Contact
Status Completed
Phase N/A
Start date November 8, 2017
Completion date November 18, 2022

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