About this trial
The use of a lumbar brace following single-level lumbar fusion for degenerative spondylosis (non-traumatic) is variable between surgeons. Some surgeons prefer to prescribe a brace and others do not. There is a lack of guidelines and evidence to support either treatment option. The purpose of this study is to assess feasibility and collect preliminary data to conduct a larger, definitive trial to provide evidence as to whether prescribing a brace or not results in better or equal outcomes. Imaging by CT scan, one year after surgery, will be used to analyze bone fusion (healing), and functional and pain scores from patients during their recovery will be compared to identify differences between patients who wore a brace and those who did not.
Eligibility criteria
Qualifiers
Single-level lumbar instrumented postero-lateral fusion from L2-L5
Life expectancy greater than 2 years
Disqualifiers
Previous lumbar surgery
Spine tumour/cancer
Documented osteoporosis
High grade (3 or 4) spondylolisthesis
Trial design
Treatments tested in this trial
- Lumbar brace
Treatment groups
Sponsors and collaborators
Hamilton Health Sciences Corporation
Lead sponsor
McMaster University
Collaborator
DJO Incorporated
Collaborator
Stryker Canada LP
Collaborator