BMX Alpha Registry: a Post-market Registry of the BioMatrix Alpha TM

Status Not yet recruiting

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

Clinical Trial Details

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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