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The Rolex Registry (Revascularization Of LEft Main With Resolute onyX) — Rolex  

Coronary Artery Disease Clinical Trial

Official title:
The ROLEX Registry (Revascularization Of LEft Main With Resolute onyX) A Multicenter Prospective Registry of the Onyx Resolute Stent for the Treatment of Unprotected Left Main Coronary Artery Disease.

Clinical Trial Summary

The primary objective of this study is to assess the safety and efficacy of the new-generation zotarolimus-eluting stent Resolute Onyx in the treatment of unprotected left main coronary artery disease (ULMCAD), both isolated or in association with two- or three-vessel coronary artery disease.

Clinical Trial Description

The ROLEX study is a prospective, non-randomized, European, multi-center registry. Four hundred and fifty patients with unprotected left main coronary artery disease (ULMCAD) will be enrolled at up to 40 European sites. The main objective of the study is to assess the safety and efficacy of the new-generation zotarolimus-eluting stent Resolute Onyx in the treatment of ULMCAD, both isolated or in association with two- or three-vessel coronary artery disease ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03316833
Study type Observational
Source University of Padova
Contact
Status Suspended
Phase
Start date November 1, 2017
Completion date December 31, 2025
View Details
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