e-BioMatrix 6 Month DAPT France

Status Completed

Clinical Trial Summary

Prospective, multi-center observational study to be conducted in up to 30 French interventional cardiology centers. The purpose of this observational study is to capture, in French Centers, clinical data of the BioMatrix Flex™ and BioMatrix NeoFlex™ Drug Eluting Coronary Stents System (Biolimus A9, BA9™-) in normal practice, in patients treated with 6-month DAPT, and to compare the outcomes to those of previous e-biomatrix registries with longer DAPT durations. The patients will be followed up for 2 years for data collection.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03461484
Study type	Observational [Patient Registry]
Source	Biosensors Europe SA
Contact
Status	Completed
Phase
Start date	March 6, 2014
Completion date	October 31, 2019

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