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Artikel im American Journal of Cardiology zeigt gute Gefäßheilung nach MiStent-SES-Implantation
Date:11/21/2013

"name">John Ormiston, M.B.Ch.B., Mercy Angiography Unit in Auckland, Neuseeland, waren die Co-Hauptprüfarzte dieser Studie.

Die DESSOLVE-II-CE-(Conformite Europeenne-)Zeichen-Studie ist eine randomisierte multizentrische Studie von Patienten mit nachgewiesener stabiler oder instabiler Angina Pectoris. Der primäre Endpunkt ist die Überlegenheit des MiStent SES bei der Minimierung des späten In-Stent-Lumenverlusts im Vergleich mit dem Medtronic Endeavor® Sprint DES, gemessen durch ein unabhängiges Angiografie-Kernlabor in De-novo-Koronarläsionen in Gefäßen mit einem Durchmesser zwischen 2,5 und 3,5 mm, geeignet für die Behandlung mit einem Stent mit einer maximalen Länge von 30 mm. In die DESSOLVE-II-Studie wurden bis zum Juli 2011 insgesamt 184 Patienten aufgenommen. Die Analyse der Daten bestätigt, dass DESSOLVE II alle Studienziele erfüllte, einen vorteilhaften späten In-Stent-Lumenverlust zeigte und ein starkes Unbedenklichkeitssignal erzielte.

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Micell Technologies verbessert mit seinen innovativen Arzneimittelgabesystemen die Leistungseigenschaften von Medizinprodukten für Herz-Kreislauf-Erkrankungen. Mit seinen einzigartigen Oberflächen- und Polymer-Bearbeitungstechnologien kann Micell die Arzneimittelfreisetzung und die Polymer-Expositionsdauer genauestens und konsistent steuern. So entstehen potenziell neue Therapielösungen für Patienten mit koronarer Herzerkrankung ohne die langfristigen Sicherheitsbedenken, mit denen derzeit am Markt erhältliche Arzneimittel-eluierende Stents behaftet sind. Darüber hinaus entwickelt Micell einen Ballon mit Arzneimittelbeschichtung für Gefäßeingriffe. Weitere Informationen erhalten Sie unter www.micell.com.

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