Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft
Stenosis, Spondylolisthesis, Degenerative Disc Disease
About this trial
This is an interventional treatment trial for Stenosis focused on measuring Primary lumbar fusion, Demineralized Bone Matrix, DBM, Optecure, Allograft, Autograft, Lumbar fusion, Interbody fusion, Instrumented fusion, Non-instrumented fusion, Exactech, Spinal fusion
Eligibility Criteria
Inclusion Criteria: Patient is indicated for primary lumbar fusion of 1 or 2 segments, L2 to S1 Patient is willing to be blindly randomized to treatment or control and remain blinded for 2 years of follow-up Patient is at least twenty-one (21) years of age Patient is expected to survive at least 2 years beyond surgery Patient is willing to participate by complying with pre- and postoperative visit requirements, including: completion of questionnaires, functional performance tests, and radiographs/CT scan Patient is willing and able to review and sign a study Informed Consent form Exclusion Criteria: Patient has a mental or physical condition that would invalidate evaluation results Patient is pregnant Patient is a prisoner Patient has a systemic infection or infection at the proposed surgical site Patient has osteopenia, osteoporosis, or osteomalacia to a degree that spinal instrumentation would be contraindicated Patient has a disease of bone metabolism Patient is undergoing chemotherapy or radiation treatment Patient is currently involved in a study of another product for a similar purpose Patient requires post-op management with nonsteroidal anti-inflammatory drugs (NSAIDs)
Sites / Locations
- Memorial Orthopaedic Surgical Group
- University of California, San Diego
- Slocum Dickson Medical Group
- State University of New York, Upstate Medical University
- NeuroSpine Solutions, P.C.
- Madigan Army Medical Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
O
A
This treatment arm includes autograft harvested from local bone and / or the iliac crest, supplemented with a demineralized bone matrix (DBM) autograft extender, Optecure.
This treatment arm includes autograft harvested from local bone and / or the iliac crest.