Low Back Pain Clinical Trial
Official title:
A Randomized, Prospective, Double-blind Controlled Evaluation of the Effectiveness of Percutaneous Lumbar Epidural Adhesiolysis and Hypertonic Saline Neurolysis
Clinically significant improvements in the percutaneous adhesiolysis patients with hypertonic
neurolysis compared to those patients randomized to the control group who did not receive
adhesiolysis and hypertonic saline neurolysis. Improvement will be assessed in relation to
the clinical outcome measures of pain and function.
Improvements among patients with adhesiolysis and hypertonic saline neurolysis and compare to
control group.
Compare adverse event profile in both groups
Patients with chronic low back pain and lower extremity pain secondary to spinal stenosis or
post lumbar laminectomy syndrome, non responsive to conservative therapy with physical
therapy or chiropractic and medical therapy and fluoroscopically directed epidural steroid
injections.
Single-center, prospective, controlled, double blind, randomized study. If non-responsive or
at patient's request, the patient may be unblinded anytime after 3 months, and will be
offered adhesiolysis and hypertonic saline neurolysis if the patient was in the control
group. All patients will be unblinded at 24 months.
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