At a glance
ClinicalIndex Comparison RecordN/ACompleted· 153 enrolled
Drug / intervention
LVIS™ and LVIS™ Jrdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Pivotal Study of the Microvention, Inc Neurovascular Self-Expanding Retrievable Stent System LVIS
In Brief
A clinical study evaluating LVIS™ and LVIS™ Jr for Intracranial Aneurysms. Completed, enrolled 153 participants across 21 sites.
Detailed Summary
The purpose of this study is to evaluate the safety and efficacy of the Low Profile Visualized Intraluminal Support(LVIS™ and LVIS™ Jr.)devices from MicroVention, Inc. when used to facilitate endovascular coiling of wide-necked intracranial aneurysms with coils.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntracranial Aneurysms
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedFeb 2013
Enrollment StartJul 2013
Primary CompletionNov 2015
Study CompletionJan 2016
TodayJul 2026
First PostedFeb 18, 2013
Enrollment StartJul 1, 2013
Primary CompletionNov 1, 2015
Study CompletionJan 1, 2016
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 13.4 years ago
Interventions
LVIS™ and LVIS™ Jrdevice
The LVIS Device is intended for use with embolization coils for the treatment of wide neck, intracranial aneurysms.