BioFreedom French Registry

Status Active, not recruiting

Clinical Trial Summary

Prospective, observational multi-center registry to be conducted at up to 25 French interventional cardiology centers. Patients will be eligible once they have received at least one BioFreedomTM DCS as per standard clinical practice and will be followed for up to 2 years post PCI for data collection. The purpose of the registry is to explore the safety and effectiveness of the BioFreedomTM DCS in standard clinical practice in France and to serve as part of Post Market Surveillance.

Clinical Trial Description

Prospective, observational multi-center registry to be conducted at up to 25 French interventional cardiology centers. Patients will be eligible once they have received at least one BioFreedomTM DCS as per standard clinical practice and will be followed for up to 2 years post PCI for data collection. The registry will be purely observational and will not interfere with physician's decisions relating to stent selection or indication for treatment. The purpose of the registry is to explore the safety and effectiveness of the BioFreedomTM DCS in standard clinical practice in France and to serve as part of Post Market Surveillance. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03745066
Study type	Observational [Patient Registry]
Source	Biosensors Europe SA
Contact
Status	Active, not recruiting
Phase
Start date	April 4, 2019
Completion date	April 27, 2022

View Details

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