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Angiographic and clinical comparison of novel Orsiro Hybrid sirolimus-eluting stents and Resolute Integrity zotarolimus-eluting stents in all-comers with coronary artery disease (ORIENT trial): study protocol for a randomized controlled trial

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dc.contributor.authorLee, Joo Myung-
dc.contributor.authorPark, Sang-Don-
dc.contributor.authorLim, Sang Yup-
dc.contributor.authorDoh, Joon-Hyung-
dc.contributor.authorCho, Jin Man-
dc.contributor.authorKim, Ki-Seok-
dc.contributor.authorBae, Jang-Whan-
dc.contributor.authorChung, Woo-Young-
dc.contributor.authorYoun, Tae-Jin-
dc.date.accessioned2021-09-05T18:57:41Z-
dc.date.available2021-09-05T18:57:41Z-
dc.date.created2021-06-15-
dc.date.issued2013-11-20-
dc.identifier.issn1745-6215-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/101586-
dc.description.abstractBackground: The Orsiro Hybrid sirolimus-eluting stent is a newly developed third-generation drug-eluting stent, featuring a unique dual-polymer mix. An active bioabsorbable polymer delivers the anti-proliferative drug, sirolimus, via controlled release, while a passive biocompatible polymeric coating shields the metallic strut from surrounding tissue, preventing interaction. To date, the Orsiro Hybrid sirolimus-eluting stent has excelled in terms of late lumen loss at 9 months in a first-in-man single-arm trial. However, the efficacy and safety data for Orsiro Hybrid sirolimus-eluting stents in a broader population of all-comers are limited. The present study offers an angiographic and clinical comparison of the Orsiro Hybrid sirolimus-eluting stent and the Resolute Integrity zotarolimus-eluting stent in the treatment of patients with coronary artery disease. Methods/design: The ORIENT trial is a multicenter, randomized, open-label, parallel-arm study designed to demonstrate the non-inferiority of the Orsiro Hybrid sirolimus-eluting stent relative to the Resolute Integrity zotarolimus-eluting stent. A total of 375 patients with a spectrum of coronary artery disease will undergo prospective, random assignment to a Orsiro Hybrid sirolimus-eluting stent or Resolute Integrity zotarolimus-eluting stent (2:1 ratio), for a primary endpoint of in-stent late lumen loss at 9 months by quantitative coronary angiography. Secondary 12-month clinical endpoints are death, target lesion revascularization, target vessel revascularization, myocardial infarction, stent thrombosis and target lesion failure (a composite of cardiac death, target lesion revascularization and target vessel-related myocardial infarction). Discussion: The ORIENT trial is the first study to date comparing the Orsiro Hybrid sirolimus-eluting stent with the Resolute Integrity zotarolimus-eluting stent for efficacy and safety in a population of all-comers with coronary artery disease.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherBMC-
dc.subjectREVASCULARIZATION-
dc.subjectOUTCOMES-
dc.subjectLESIONS-
dc.titleAngiographic and clinical comparison of novel Orsiro Hybrid sirolimus-eluting stents and Resolute Integrity zotarolimus-eluting stents in all-comers with coronary artery disease (ORIENT trial): study protocol for a randomized controlled trial-
dc.typeArticle-
dc.contributor.affiliatedAuthorLim, Sang Yup-
dc.identifier.doi10.1186/1745-6215-14-398-
dc.identifier.scopusid2-s2.0-84887660175-
dc.identifier.wosid000328753600005-
dc.identifier.bibliographicCitationTRIALS, v.14-
dc.relation.isPartOfTRIALS-
dc.citation.titleTRIALS-
dc.citation.volume14-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusREVASCULARIZATION-
dc.subject.keywordPlusOUTCOMES-
dc.subject.keywordPlusLESIONS-
dc.subject.keywordAuthorDrug-eluting stent-
dc.subject.keywordAuthorOrsiro hybrid stent-
dc.subject.keywordAuthorZotarolimus-eluting stent-
dc.subject.keywordAuthorCoronary heart disease-
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