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MiStent SES erweist sich im klinischen Umfeld als einzigartig
Date:10/28/2013

rschungsleiter dieser Studie.

Die DESSOLVE II-Studie zur CE-Zulassung (Conformite Europeenne) ist eine randomisierte, multizentrische Studie an Patienten mit nachweislich stabiler bzw. instabiler Angina Pectoris. Der primäre Endpunkt ist die Überlegenheit des MiStent SES bei der Minimierung von spätem In-Stent-Lumenverlust nach neun Monaten gegenüber Medtronics Endeavor® Sprint DES. Maßgeblich sind die aus einem unabhängigen Angiografielabor stammenden Messwerte von de-novo-Koronarläsionen in Gefäßen mit 2,5 bis 3,5 mm Durchmesser bei Patienten, für die eine Behandlung mit einem Stent mit maximaler Länge von 30 mm infrage kam. Die Aufnahme von 184 Patienten in die Studie DESSOLVE II wurde im Juli 2011 abgeschlossen. Die Auswertung der Daten bestätigt, dass alle Untersuchungsziele der Studie DESSOLVE II erfüllt wurden. Im Zuge der Studie wurde ein wettbewerbsfähiger später In-Stent-Lumenverlust festgestellt und zudem ein hohes Sicherheitsniveau erreicht.

Informationen zu Micell Technologies Inc.

Micell Technologies ist ein biomedizinisches Unternehmen, das die Leistung kardiovaskulärer Medizingeräte mit innovativen Systemen zur Verabreichung von Medikamenten optimiert. Seine einzigartigen Technologien zur Oberflächen- und Polymermodifikation versetzen Micell in die Lage, die Wirkstofffreisetzung und Dauer der Polymerexposition präzise und beständig zu steuern. Daraus ergibt sich das Potenzial, eine therapeutische Lösung zur Behandlung der koronaren Herzkrankheit ganz ohne die langfristigen Sicherheitsprobleme zu entwickeln, die mit derzeit verfügbaren Medikamente freisetzenden Stents einhergehen. Micell entwickelt zudem einen mit Medikamenten beschichteten Ballon für vaskuläre Eingriffe. Besuchen Sie uns auf www.micell.com.

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