# VISIBILITY™ Iliac Study

> **NCT01402700** · NA · COMPLETED · sponsor: **Medtronic Endovascular** · enrollment: 75 (actual)

## Conditions studied

- Peripheral Arterial Disease
- Claudication

## Interventions

- **DEVICE:** Visi-Pro™ Balloon Expandable Stent System

## Key facts

- **NCT ID:** NCT01402700
- **Lead sponsor:** Medtronic Endovascular
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2011-07
- **Primary completion:** 2013-07
- **Final completion:** 2015-09
- **Target enrollment:** 75 (ACTUAL)
- **Last updated:** 2018-03-07


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01402700

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01402700, "VISIBILITY™ Iliac Study". Retrieved via AI Analytics 2026-09-03 from https://api.ai-analytics.org/clinical/NCT01402700. Licensed CC0.

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