Viewing Study NCT00264043



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Last Modification Date: 2024-10-26 @ 9:21 AM
Study NCT ID: NCT00264043
Status: COMPLETED
Last Update Posted: 2008-08-06
First Post: 2005-12-09

Brief Title: The Study to Evaluate Patient Outcome Using Distal Protection Combined With the BX Velocity
Sponsor: Cordis Corporation
Organization: Cordis Corporation

Study Overview

Official Title: Distal Protection Combined With Velocity in Coronary Arteries and SVBG Registry
Status: COMPLETED
Status Verified Date: 2008-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: DISCOVER
Brief Summary: The primary objective is to evaluate the use of the AngioGuard device combined with the Bx Velocity on patient outcome at one month
Detailed Description: This is a prospective non-randomized multi-center trial Patients will be treated with the AngioGuard device and Bx Velocity stent and will be followed for six-months post-procedure

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None