Trial to Evaluate the Safety & Efficacy of the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery

Completed · Phase 3

Conditions studied: Peripheral Vascular Disease

In brief

To determine the safety and efficacy of the Omnilink Elite™ Peripheral Balloon-Expandable Stent System in subjects with atherosclerotic de novo or restenotic lesions in the native common iliac artery and/or native external iliac artery.

Key facts

Study ID

NCT01396525

Run by

Abbott Medical Devices

People needed

153

Starts

2009-03-01

Expected to finish

2014-06-01

Last updated by the study team

2016-02-08

Who can join

Age: 18 and older, up to 89. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Abbott Vascular — Santa Clara, California, United States

Full record on ClinicalTrials.gov

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