At a glance
ClinicalIndex Comparison RecordN/ACompleted· 75 enrolled
Drug / intervention
Visi-Pro™ Balloon Expandable Stent Systemdevice
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.
Visi-Pro™ Balloon Expandable Iliac Study (VISIBILITY™ Iliac)
In Brief
A clinical study evaluating Visi-Pro™ Balloon Expandable Stent System for Peripheral Arterial Disease and Claudication. Completed, enrolled 75 participants across 1 site.
Detailed Summary
The VISIBILITY Iliac study is a prospective, multi-center, non-randomized study confirming the safety and effectiveness of stenting using the Visi-Pro™ Balloon Expandable Stent System for the treatment of stenotic, restenotic or occluded lesions in the common and external iliac artery.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPeripheral Arterial Disease, Claudication
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartJul 2011
First PostedJul 2011
Primary CompletionJul 2013
Study CompletionSep 2015
TodayJul 2026
First PostedJul 26, 2011
Enrollment StartJul 1, 2011
Primary CompletionJul 1, 2013
Study CompletionSep 1, 2015
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 14.9 years ago
Interventions
Visi-Pro™ Balloon Expandable Stent Systemdevice
Implantation of one or more study devices in the common and/or external iliac artery.