Absolute Pro® MOMENTUM™
Completed · Not applicable
Conditions studied: Peripheral Artery Disease, Peripheral Vascular Disease
In brief
To evaluate the safety and effectiveness of the Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent System for the treatment of subjects with atherosclerotic de novo or restenotic lesions in the native superficial femoral artery (SFA) and/or the native proximal popliteal artery (PPA). CAUTION: Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent Systems are investigational devices. Limited by Federal (U.S.) law to investigational use only.
Key facts
- Study ID
- NCT01444378
- Run by
- Abbott Medical Devices
- People needed
- 141
- Starts
- 2011-10-01
- Expected to finish
- 2015-05-01
- Last updated by the study team
- 2017-06-06
Who can join
Age: 18 and older. 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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