Last updated on August 2020

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


Brief description of study

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.

Clinical Study Identifier: NCT04138238

Find a site near you

Start Over

H pital Priv Claude Galien

Quincy-sous-Sénart, France
  Connect »

Segeberg Kliniken

Bad Segeberg, Germany
  Connect »

UKSH

Kiel, Germany
  Connect »

Klinikum Wilhelmshaven

Wilhelmshaven, Germany
  Connect »

H pital Priv Claude Galien

Quincy-sous-Sénart, France
  Connect »

Kantonsspital St. Gallen

Saint Gallen, Switzerland
  Connect »

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


Volunteer Sign-up

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.