Clinical trial
A Prospective, Non-randomized, Two Arm, Multi-center Clinical Trial to Evaluate the Safety and Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System and 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.
NCT01396525 is registered in ClinicalTrials.gov with Abbott Medical Devices as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Prospective, Non-randomized, Two Arm, Multi-center Clinical Trial to Evaluate the Safety and Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System and 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.
- Lead sponsor
- Abbott Medical Devices
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- March 31, 2009
- Completion date
- June 30, 2014
- Enrollment
- 153 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
peripheral vascular disease