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Post-Approval Study of the NexStent Carotid Stent System and the FilterWire EZ Embolic Protection System: SONOMA — SONOMA  

Carotid Stenosis Clinical Trial

Official title:
The NexStent® Carotid Stent System: A Post Market Approval Evaluation Study In Conjunction With the FilterWire EZ™ Embolic Protection System

Clinical Trial Summary

The primary objective of the SONOMA Registry is to confirm the safety of the NexStent® Carotid Stent System and FilterWire EZ™ Embolic Protection System in routine clinical practice and to identify rare or unanticipated device-related events that might occur.

Clinical Trial Description

The SONOMA Registry will enroll approximately 300 subjects at a maximum at 78 study centers. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00478673
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Terminated
Phase Phase 4
Start date May 2007
Completion date July 2009
View Details
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