Pilot Study to Assess Safety/Preliminary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion Surgery



Status:Archived
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:November 2008
End Date:May 2011

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Trial Summary
Trial Overview
Inclusion Criteria

A Multi-Center, Prospective, Parallel Group, Randomized, Pilot Study Evaluating Safety and Preliminary Effectiveness Of Prefix Compared To Iliac Crest Bone In Subjects With DDD Undergoing Transforaminal Lumbar Interbody Fusion


This is a pilot study to evaulate the safety and prelimary effectiveness of Prefix as
compared to autogenous bone for spinal fusion procedures in skeletally mature subjects with
degenerative disc disease (DDD) at one level from L2-S1.



We found this trial at
7
sites
University of Kansas Medical Center
3901 Rainbow Blvd
Kansas City, Kansas 66160
(913) 588-5000
University of Kansas Medical Center The University of Kansas Medical Center serves Kansas through excellence...
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Kansas City, KS
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Confidential
Indianapolis, Indiana 46237
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Indianapolis, IN
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Confidential
Jefferson City, Missouri 65101
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Jefferson City, MO
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Johnson City, New York 13790
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Johnson City, NY
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Tyler, Texas 75701
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Tyler, TX
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St. Elizabeth Children's Health Center
Utica, New York 13502
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Utica, NY
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Confidential
Washington, Washington DC 20037
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Washington, DC
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