Indiana Spine Group and Rick Sasso, MD, Principal Investigator, are conducting a study to evaluate the safety and efectiveness of the ACADIA® Facet Replacement System FOR THOSE SUFFERING FROM BACK AND LEG PAIN AND DIFFICULTY WALKING CAUSED BY LUMBAR SPINAL STENOSIS (LSS). ACADIA® is an
You May Qualify for a Lumbar Spinal Stenosis Research Study
investigational device for the surgical treatment of LSS without fusion, designed to maintain the motion of the spine. Indiana Spine Group is one of only 30 sites in the U.S. approved to enroll patients in the ACADIA® study. To participate in the study, patients must • Be between the ages of 21-85 • Be diagnosed with Lumbar Spinal Stenosis • Have undergone at least 6 months of non- surgical treatment (e.g., injections, physical therapy, medications, etc.)
For more information on the ACADIA® study, please call Indiana Spine Group at
317-715-5897 or email Sheetal Vinayek, Clinical Research Coordinator, at svinayek@indianaspinegroup.com.
Indiana Spine Group • 13225 N. Meridian Street • Carmel, IN
CALL: 844-4RESTOR
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TownePost.com / FEBRUARY 2015 / TOWNEPOST NETWORK
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