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TWENTE Study: The Real-World Endeavor Resolute Versus Xience V Drug-Eluting Stent Study in Twente: study design, rationale and objectives
Authors:M. W. Z. Basalus  K. Tandjung  K. G. van Houwelingen  M. G. Stoel  F. H. A. F. de Man  J. W. Louwerenburg  S. A. M. Saïd  G. C. M. Linssen  M. A. W. J. Kleijne  J. van der Palen  J. Huisman  P. M. J. Verhorst  C. von Birgelen
Affiliation:1. Department of Cardiology, Thoraxcentrum Twente, Medisch Spectrum Twente, PO Box 50 000, 7500, KA, Enschede, the Netherlands
2. www.bsl.nl/shop/
Abstract:Background. New-generation drug-eluting stents (DES) may solve several problems encountered with first-generation DES, but there is a lack of prospective head-to-head comparisons between new-generation DES. In addition, the outcome of regulatory trials may not perfectly reflect the outcome in ‘real world’ patients. Objectives. To compare the efficacy and safety of two new-generation DES in a ‘real world’ patient population. Methods. A prospective, randomised, single-blinded clinical trial to evaluate clinical outcome after Endeavor Resolute vs. Xience V stent implantation. The primary endpoint is target vessel failure at one-year follow-up. In addition, the study comprises a two-year and an open-label five-year follow-up. (Neth Heart J 2010;18:360-4.)
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