Viewing Study NCT01793792



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Last Modification Date: 2024-10-26 @ 11:03 AM
Study NCT ID: NCT01793792
Status: COMPLETED
Last Update Posted: 2019-11-27
First Post: 2013-02-14

Brief Title: Pivotal Study of the LVIS Low Profile Visualized Intraluminal Support
Sponsor: Microvention-Terumo Inc
Organization: Microvention-Terumo Inc

Study Overview

Official Title: Pivotal Study of the Microvention Inc Neurovascular Self-Expanding Retrievable Stent System LVIS
Status: COMPLETED
Status Verified Date: 2019-11
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: LVIS
Brief Summary: The purpose of this study is to evaluate the safety and efficacy of the Low Profile Visualized Intraluminal SupportLVIS and LVIS Jrdevices from MicroVention Inc when used to facilitate endovascular coiling of wide-necked intracranial aneurysms with 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
Secondary IDs
Secondary ID Type Domain Link
G110188S004 OTHER FDA None