NCT00753337

The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study

The ACTIVE (Use of the Assurant® Cobalt Iliac Stent System in the Treatment of Iliac Vessel Disease) Study Using the Medtronic Assurant Cobalt Iliac Balloon-Expandable Stent System

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 123 (actual)
• Sponsor: Medtronic Endovascular · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The objective of this study is to evaluate the safety and efficacy of the Assurant Cobalt Iliac Stent System in the treatment of de novo and restenotic lesions in iliac arteries of subjects with Peripheral Artery Disease (PAD).

Detailed description

This study is being conducted to collect 9 month safety and efficacy data on the Assurant Cobalt Iliac Stent for all subjects enrolled into the study.

Conditions

• Peripheral Vascular Disease

Interventions

Type	Name	Description
DEVICE	Assurant® Cobalt Iliac Stent System	Iliac Stenting

Timeline

• Start date: 2008-10-01
• Primary completion: 2011-02-01
• Completion: 2013-09-01
• First posted: 2008-09-16
• Last updated: 2016-04-04
• Results posted: 2013-12-30

Locations

2 sites across 1 country: United States