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Stenting and Angioplasty With Protection in Patients at High Risk for Endarterectomy (SAPPHIRE)

Carotid Artery Disease Clinical Trial

Official title:
Stenting and Angioplasty With Protection in Patients at High Risk for Endarterectomy

Clinical Trial Summary

The primary objective of this study is to compare the safety and effectiveness of the Cordis Nitinol Carotid Stent and Delivery Systems (5.5 F and 7 F) with the ANGIOGUARD XP distal protective device to CEA in the treatment of carotid artery disease in patients at increased risk for surgery.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00231270
Study type Interventional
Source Cordis Corporation
Contact
Status Completed
Phase Phase 3
Start date August 2000
Completion date August 2005
View Details
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