ObjectivesThis study sought to compare clinical outcomes and angiographic findings using the Resolute zotarolimus-eluting stent (R-ZES) (Medtronic, Santa Rosa, California) versus the Taxus Liberte paclitaxel-eluting stent (PES) (Boston Scientific, Natick, Massachusetts) in an all-comer Chinese population.BackgroundConcerns regarding restenosis risk led to new-generation drug-eluting stents (DES) designed for use in patients with complex clinical or lesion characteristics. In-stent late lumen loss (LLL) is a measure of restenosis risk.MethodsPatients with an indication for treatment with a DES were randomized in a 1:1 ratio to placement of at least 1 R-ZES or PES with minimal exclusions. The primary endpoint was angiographic in-stent LLL at ...
ObjectivesThe aim of this study was to evaluate the relative efficacy and safety of zotarolimus-elut...
ObjectivesA novel zotarolimus-eluting coronary stent system (ZoMaxx, Abbott Laboratories, Abbott Par...
ObjectivesOur purpose was to make a synthesis of the available evidence on the relative efficacy and...
ObjectivesThis study sought to compare clinical outcomes and angiographic findings using the Resolut...
ObjectivesThe aim of this study was to compare the safety and efficacy of Resolute zotarolimus-eluti...
The RESOLUTE China Registry is a prospective, multicenter, all-comers, observational study of patien...
ObjectivesThis trial examined the relative clinical efficacy, angiographic outcomes, and safety of z...
First-generation drug-eluting stents (DESs) have reduced angiographic and clinical restenosis rates ...
ObjectivesThe aim of this study was to examine outcomes related to the use of the Endeavor zotarolim...
ObjectivesThe aim of this study was to evaluate late safety and efficacy outcomes among patients enr...
ObjectivesThe purpose of this study was to compare the 9-month clinical outcomes of patients treated...
ObjectivesThis study sought to compare the safety and efficacy of the Xience V/Promus everolimus-elu...
SummaryBackgroundThe zotarolimus-eluting stent (ZES) is a new drug-eluting stent that delivers zotar...
ObjectivesThis study sought to compare late safety and efficacy outcomes following percutaneous coro...
ObjectivesThis study sought to assess the clinical safety and effectiveness of the Resolute zotaroli...
ObjectivesThe aim of this study was to evaluate the relative efficacy and safety of zotarolimus-elut...
ObjectivesA novel zotarolimus-eluting coronary stent system (ZoMaxx, Abbott Laboratories, Abbott Par...
ObjectivesOur purpose was to make a synthesis of the available evidence on the relative efficacy and...
ObjectivesThis study sought to compare clinical outcomes and angiographic findings using the Resolut...
ObjectivesThe aim of this study was to compare the safety and efficacy of Resolute zotarolimus-eluti...
The RESOLUTE China Registry is a prospective, multicenter, all-comers, observational study of patien...
ObjectivesThis trial examined the relative clinical efficacy, angiographic outcomes, and safety of z...
First-generation drug-eluting stents (DESs) have reduced angiographic and clinical restenosis rates ...
ObjectivesThe aim of this study was to examine outcomes related to the use of the Endeavor zotarolim...
ObjectivesThe aim of this study was to evaluate late safety and efficacy outcomes among patients enr...
ObjectivesThe purpose of this study was to compare the 9-month clinical outcomes of patients treated...
ObjectivesThis study sought to compare the safety and efficacy of the Xience V/Promus everolimus-elu...
SummaryBackgroundThe zotarolimus-eluting stent (ZES) is a new drug-eluting stent that delivers zotar...
ObjectivesThis study sought to compare late safety and efficacy outcomes following percutaneous coro...
ObjectivesThis study sought to assess the clinical safety and effectiveness of the Resolute zotaroli...
ObjectivesThe aim of this study was to evaluate the relative efficacy and safety of zotarolimus-elut...
ObjectivesA novel zotarolimus-eluting coronary stent system (ZoMaxx, Abbott Laboratories, Abbott Par...
ObjectivesOur purpose was to make a synthesis of the available evidence on the relative efficacy and...