Three hundred and 34 patients in the SAPPHIRE study were randomized to either CAS or CEA. Therefore, patients receiving CAS with precise? Nitinol Self-Expanding Stent and ANGIOGUARDTM XP Emboli Capture Guidewire System maintained a low incidence of stroke after the first 30 days for the duration of the three-year follow-up in the USFS and SAPPHIRE tablette substance active . In the SAPPHIRE study at 36 months the incidence of stroke was virtually identical for both CAS and CEA (7.1 percent for CAS and 6.7 percent for CEA, The 3-year incidence of stroke across the randomized and non – randomized CAS treatment groups in SAPPHIRE and the USFS had only an average increase of 4.0 percent over the 30-day stroke rate. Cordis Corporation, a Johnson & Johnson company, sponsored the SAPPHIRE and USFS clinical trials. Jay S The Cleveland Clinic Foundation, and Principal said investigator for the SAPPHIRE study: The SAPPHIRE study showed CAS was not inferior to CEA This is important new data which suggests the long-term durability of CAS in this patient population. .

Cordis Endovascular, a division of Cordis Corporation, is a leader in endovascular diagnostic catheters and a recognized leader in endovascular education, research and development. The company has the resources to develop and launch breakthrough treatments and a history of delivering reliable, high quality products to customers and patients.

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