Projekt

Cruz HBR

Abgeschlossen · 2020 bis 2022

Art
Klinische Forschung
Reichweite
Multizentrisch, KSSG als teilnehmendes Zentrum
Bereiche
Status
Abgeschlossen
Start
2020
Ende
2022
Finanzierungsart
Industrie
Studiendesign
Prospective, multi-center, open-label, single-arm registry designed to enroll 1200 (800 non-High Bleeding Risk (non-HBR) and 400 HBR) allcomer patients with coronary artery disease in around 25 sites in 3 European countries (Switzerland, Germany & France). Patients will receive at least one Supraflex Cruz™ sirolimus-eluting stent as per current practice and will be followed up for 12 months.
Kurzbeschreibung/Zielsetzung

Post-market registry to evaluate the safety and efficacy of the Supraflex Cruz™ sirolimus-eluting coronary stent system in the treatment of all-comer patients with coronary artery disease