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Cruz HBR Registry - Post-market Registry to Evaluate the Safety and Efficacy of the Supraflex Cruz Stent

2019-10-29 14:36:42 | BioPortfolio

Summary

This is a prospective, multicenter, open-label, single-arm registry. The primary objective of this registry is to confirm the results of the Supraflex Cruz stent in real life all-comer patients (800 patients as in the Supraflex arm of the TALENT trial) and demonstrate that the Supraflex Cruz stent is not inferior to the BioFreedom stent in High Bleeding Risk (HBR) patients (400 patients) with respect to device oriented composite endpoint (DOCE) at 12 months. All patients will be followed up to 12 months after the index procedure.

Study Design

Conditions

Coronary Artery Disease

Intervention

Supraflex Cruz Sirolimus-eluting Stent

Location

Grand Hôpital de l'Est Francilien - CH de Lagny Marne la Vallée
Jossigny
France
77600

Status

Not yet recruiting

Source

Sahajanand Medical Technologies Pvt. Ltd.

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-10-29T14:36:42-0400

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Medical and Biotech [MESH] Definitions

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