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ABSTRACT: Background and objectives
To compare the safety and efficacy of a new everolimus-eluting stent with an abluminal-coated biodegradable polymer (Osstem Cardiotec Centum) with those of the Xience Alpine stent (Xience).Methods
This randomized, prospective, multicenter, parallel-designed, single-blind trial was conducted among patients with myocardial ischemia undergoing percutaneous coronary intervention (PCI) from 21st September 2018 until 3rd July 2020. The primary efficacy endpoint was in-segment late lumen loss (LLL) at 270 days after the procedure and the primary safety endpoints were major adverse cardiac events (MACE), composite of cardiac death, myocardial infarction, and target lesion revascularization.Results
We enrolled 121 patients and analyzed 113 patients
SUBMITTER: Yoon CH
PROVIDER: S-EPMC9064698 | biostudies-literature | 2022 May
REPOSITORIES: biostudies-literature