This is a single-center study evaluating the outcomes of patients with painful lumbar spinal stenosis who were treated with the mild procedure (minimally invasive lumbar decompression. The patients will be followed for 6 months after the procedure.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Symptomatic and lumbar spinal stenosis caused by dorsal element hypertrophy
* Prior failure of conservative therapy and Oswestry Disability Index (ODI) \>20%
* Radiologic evidence of lumbar spinal stenosis, ligamentum flavum hypertrophy (typically \>2.5mm),confirmed by pre-op MRI/CT report
* Central canal cross sectional area clearly reduced per MRI/CT report
* If present, anterior listhesis \< or = to 5.0mm (preferred) and deemed stable by the Investigator
* Able to walk at least 10 feet unaided before being limited by pain
* Available to complete 26 weeks of follow up
* A signed Consent Form is obtained from the patient
* Adults 18 years of age or older
Exclusion Criteria:
* Prior surgery at the intended treatment level
* Compound fracture with intraspinal retropulsion contributing to spinal stenosis
* Disabling back or leg pain from causes other than lumbar spinal stenosis
* Disc protrusion or osteophyte formation severe enough to confound study outcome
* Facet hypertrophy severe enough to confound study outcome
* Bleeding disorders and/or current use of anti-coagulants
* Use of acetylsalicylic acid (ASA) and/or non-steroidal anti-inflammatory drug (NSAID) within 5 days of treatment
* Epidural steroids with 3 weeks prior to procedure
* Inability of patient to lie prone for any reason with anesthesia support
* Metabolic wound healing pathologies that may be deemed by the Investigator to compromise the study outcomes
* Dementia and/or inability to gi…