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The purpose of the STROLL study is to test the safety and effectiveness of the SMART stent in patients with blockages in their legs.

To be eligible for the STROLL study, you must:

• Be 30 years old or above
• Leg pain
• Have a blockage in the superficial femoral artery that can be fixed with a stent

For more information, please contact Rebecca Morrissey at 414-649-3356 or email at rmorrissey@hrtcare.com

Principal Investigator: Dr. Tanvir Bajwa

Clinical trial location(s)

Aurora St. Luke's Medical Center
2900 West Oklahoma Avenue
Milwaukee, WI 53215

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