Ignite Creation Date:
2024-05-06 @ 2:47 AM
Last Modification Date:
2024-10-26 @ 11:23 AM
Study NCT ID:
NCT02125097
Status:
COMPLETED
Last Update Posted:
2019-01-11
First Post:
2014-04-22
Brief Title:
The Reverse Barrel VRD Intracranial Aneurysm Trial
Sponsor:
Medtronic Neurovascular Clinical Affairs
Organization:
Medtronic Neurovascular Clinical Affairs
Study Overview
Official Title:
Multi-center Non-randomized Clinical Investigation of the Reverse Medical Barrel Vascular Reconstruction Device VRD for Adjunctive Treatment to Embolic Coils for Wide Neck Intracranial Bifurcation and Branch Aneurysms
Status:
COMPLETED
Status Verified Date:
2019-01
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:
Barrel
Brief Summary:
The purpose of this clinical investigation is to evaluate the safety and effectiveness of the Barrel VRD when used to facilitate endovascular coiling of wide-neck bifurcating or branch intracranial aneurysms with any approved embolic coils
Detailed Description:
None
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