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VISIBILITY™ Iliac Study

NCT01402700 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2018-03-07

Study results available
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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

  • Peripheral Arterial Disease
  • Claudication

Interventions

DEVICE

Visi-Pro™ Balloon Expandable Stent System

Implantation of one or more study devices in the common and/or external iliac artery.

Sponsors & Collaborators

  • Medtronic Endovascular

    lead INDUSTRY

Principal Investigators

  • Peter L. Faries, M.D. · Icahn School of Medicine at Mount Sinai

  • John H. Rundback, M.D. · Holy Name Medical Center

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-07-31
Primary Completion
2013-07-31
Completion
2015-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01402700 on ClinicalTrials.gov