At a glance
ClinicalIndex Comparison RecordN/ACompleted· 138 enrolled
Drug / intervention
BARREL VRDdevice
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.
Prospective, Multi-Center, Single-Arm Study of Reverse Medical Barrel™ Vascular Reconstruction Device for Adjunctive Treatment to Embolic Coils in Wide-Neck, Intracranial, Bifurcating Aneurysms of Middle Cerebral and Basilar Arteries
In Brief
A clinical study evaluating BARREL VRD for Intracranial Bifurcating Aneurysms. Completed, enrolled 138 participants across 3 sites.
Detailed Summary
Single arm study to evaluate the outcomes of treatment with the Barrel VRD device as an adjunctive treatment to coiling for wide neck, intracranial, bifurcating/branching aneurysms in the middle cerebral and basilar arteries.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIntracranial Bifurcating Aneurysms
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJul 2014
Enrollment StartOct 2014
Primary CompletionJul 2017
TodayJul 2026
First PostedJul 1, 2014
Enrollment StartOct 13, 2014
Primary CompletionJul 21, 2017
TodayJul 2, 2026
Enrollment to primary: 2.8 yearsPosted 12.0 years ago
Interventions
BARREL VRDdevice
The Barrel VRD was implanted as adjunctive to embolic coils in subjects with wide necked bifurcating aneurysms within the Middle Cerebral and Basilar Arteries.