Prospective Randomized Three Arm Study of lumbar Spinal Fusion Graft Efficacy: Bone marrow aspirate concentrate & Allograft versus Recombinant Bone Morphogenetic Protein-2 (BMP) versus Control Group
Are you eligible to participate in this study?
You may be eligible for this study if you meet the following criteria:
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Conditions: Spinal Disease
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Age: Between 18 Year(s) - 100 Year(s)
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Gender: Male or Female
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Other Inclusion Criteria:
- Scheduled for elective posterior or anterior and posterior spinal fusion of the thoracolumbar spine with or without anterior interbody support.
- Failed at least 6 weeks of conservative care
- Oswestry Disability Index (ODI) score > 30%
- No contraindication to BMAC (as per manufacturer)
You may not be eligible for this study if the following are true:
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- Prior lumbar fusion surgery at operative level (prior discectomy and/or laminectomy allowed)
- Spondylolisthesis grade 3 or more
- Incompetent or missing anterior arch at the affected level (e.g. laminectomy, pars defect)
- Currently requires laminectomy at level of surgery
- Facet joints at implant level are absent or fractured
- Post-traumatic vertebral body compromise or acute fracture at implant level
- Body mass Index (BMI) > 40
- Known allergy to titanium
- Paget’s disease, osteomalacia, or any other metabolic bone disease
- Use of medications or any drug known to potentially interfere with bone/soft tissue healing (e.g. chronic systemic steroids)
- Dentato Rubro Thalamic Tract (drtt)
- Subject has recent history (less than 3 years) of chemical substance dependency or significant psychosocial disturbance that may impact the outcome or study participation
- Participation in a clinical trial of another investigational drug or device within the past 30 days
- Systemic infection such as AIDS, HIV, and active hepatitis
- Active malignancy defined as history of invasive malignancy
- Pregnant or planning to become pregnant during the length of study participation
- Involvement in active litigation related to back problems at the time of screening (this does not apply to litigation required by no fault states)
- Direct involvement in the execution of this protocol
- Intraoperative exclusion: Any change in the surgical procedure PRIOR to surgery that violates the inclusion/exclusion criteria.
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.