Trials / Completed
CompletedNCT01402700
VISIBILITY™ Iliac Study
Visi-Pro™ Balloon Expandable Iliac Study (VISIBILITY™ Iliac)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 75 (actual)
- Sponsor
- Medtronic Endovascular · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Visi-Pro™ Balloon Expandable Stent System | Implantation of one or more study devices in the common and/or external iliac artery. |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2013-07-01
- Completion
- 2015-09-01
- First posted
- 2011-07-26
- Last updated
- 2018-03-07
- Results posted
- 2015-09-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01402700. Inclusion in this directory is not an endorsement.