The purpose of the study is to demonstrate safety and efficacy of spinal cord stimulation with peripheral nerve field stimulation for the treatment of chronic low back and leg pain.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
38
Spinal Cord Stimulation (SCS) in combination with Peripheral Nerve Field Stimulation (PNfS). The SCS leads will be placed in the Thoracolumbar region and the PNfS lead will be placed subcutaneously in the area of pain.
Spinal Cord Stimulation (SCS) only. The SCS leads will be placed in the Thoracolumbar region only.
Safety
Evaluation of device or procedure related adverse events
Time frame: 6 months
Efficacy
Responder rate in SCS-PNfS vs SCS alone
Time frame: 3 months
Quality of Life
Time frame: 3 months
Functional Disability
Time frame: 3 months
Worst pain
Time frame: 3 months
Rescue medication usage
Time frame: 3 months
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