Ignite Creation Date:
2024-05-05 @ 5:25 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00453518
Status:
COMPLETED
Last Update Posted:
2009-08-18
First Post:
2007-03-28
Brief Title:
The RETRIEVE Study Use of the FiberNet Embolic Protection System in Saphenous Vein Grafts
Sponsor:
Lumen Biomedical
Organization:
Lumen Biomedical
Study Overview
Official Title:
Evaluating the Use of the FiberNet Embolic Protection System in Saphenous Vein Grafts The RETRIEVE Study
Status:
COMPLETED
Status Verified Date:
2009-08
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:
RETRIEVE
Brief Summary:
This is a multicenter prospective study designed to demonstrate the performance and safety of the FiberNet Embolic Protection System when used as an adjunctive device during saphenous vein graft SVG intervention
Detailed Description:
The study will involve up to 30 patients to be enrolled using the FiberNet device during clinically indicated percutaneous intervention of SVG and followed through 30 days post procedure Patients will be enrolled at up to 10 Investigative Sites The study is a prospective multi-center registry with sequential enrollment of qualified patients who consent to participate and meet all entrance criteria
The Lumen Biomedical Inc FiberNet Embolic Protection System is indicated for use as a guide wire and embolic protection system to capture and remove embolic material thrombusdebris produced while performing percutaneous transluminal interventional procedures in saphenous vein grafts with reference vessel diameters of 175 mm to 70 mm
The Lumen Biomedical Inc FiberNet Embolic Protection System is indicated for use as a guide wire and embolic protection system to capture and remove embolic material thrombusdebris produced while performing percutaneous transluminal interventional procedures in saphenous vein grafts with reference vessel diameters of 175 mm to 70 mm
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