NCT01402700View on ClinicalTrials.gov

VISIBILITY™ Iliac Study

NACompletedINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

July 31, 2011

Primary Completion Date

July 31, 2013

Study Completion Date

September 30, 2015

Conditions
Peripheral Arterial DiseaseClaudication
Interventions
DEVICE

Visi-Pro™ Balloon Expandable Stent System

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

Trial Locations (1)

Unknown

Holy Name Medical Center, Teaneck

Sponsors
All Listed Sponsors
lead

Medtronic Endovascular

INDUSTRY

NCT01402700 - VISIBILITY™ Iliac Study | Biotech Hunter | Biotech Hunter