WebThe XIENCE Skypoint™, XIENCE Sierra™ and XIENCE Alpine™ Stent Systems are contraindicated for use in: Patients who cannot tolerate, including allergy or hypersensitivity to, procedural anticoagulation or the post-procedural antiplatelet regimen. WebKedhi E, Latib A, Abizaid A, et al. Rationale and design of the Onyx ONE global randomized trial: A randomized controlled trial of high bleeding risk patients after stent placement with 1 month of dual antiplatelet therapy. Am Heart J. August 2024;214:134-141.
Medtronic MRI Resource Library: Home
Web17 de abr. de 2015 · A Clinical Evaluation of the Medtronic Resolute Onyx Zotarolimus-Eluting Stent System Medtronic RESOLUTE ONYX Core (2.25 mm - 4.0 mm) Clinical Study: Actual Study Start Date : July 7, 2015: Actual Primary Completion Date : July 5, 2016: Actual Study Completion Date : December 3, 2024: WebBACKGROUND: Bifurcation lesions in coronary arteries are complex to treat with coronary stents, which are not designed for that purpose and can be unproperly deployed. Moreover, devices are constantly evolving, and so are angioplasty techniques. OBJECTIVES: The aim of this study was to determine the performances of different stents in the treatment of … incitement to mutiny act 1797
A Randomized Controlled Trial with Resolute Onyx in One Month …
Web1 de out. de 2024 · The Resolute Onyx DES is the first-and-only DES in the U.S. that has been proven safe and effective utilizing a one-month regimen of DAPT – the combination of aspirin and an anti-clotting medication – following a percutaneous coronary intervention (PCI) in patients at high bleeding risk. WebIm August 2024 brachte Medtronic seinen Onyx Frontier Drug-Eluting Stent (DES) auf den Markt, ein neues interventionelles Angebot für die koronare Herzkrankheit (KHK), das mit einem aktualisierten Abgabesystem, verbesserter Flexibilität und einem geringeren Crossing-Profil ausgestattet ist. Web13 de abr. de 2024 · In August 2024: Following the CE Mark's approval, Medtronic introduced the Onyx Frontier drug-eluting stent in Europe in August 2024. In May 2024 : The FDA granted Medtronic plc approval for the ... inbounddetour