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Clinical Trial Summary

Prospective, multi-center, registry designed to enrol up to 2,000 patients in up to 35 International centers. All patients will receive a BioMatrix AlphaTM stent as per clinical practice and will be followed for 2 years for data collection. Major adverse cardiac events (MACE) results at 9 months will be compared to the results obtained from the BioMatrix FlexTM arm of the LEADERS trial.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02871622
Study type Observational [Patient Registry]
Source Biosensors Europe SA
Contact Diana Schuette
Phone +447 970 942 022
Email d.schuette-consultant@biosensors.com
Status Not yet recruiting
Phase N/A
Start date September 2016
Completion date October 2019

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