The purpose of this study is to compare standard of care treatments for back pain to electrical stimulation. Stimulation is delivering small amounts of electricity to the nerves in your low back. This study will use a device called the SPRINT Peripheral Nerve Stimulation (PNS) System. The device is cleared by the FDA for up to 60 days of use for the relief of chronic or acute pain (including back pain)
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Reduction in average pain intensity
Timeframe: Up to 3-months after Start of Therapy (SOT)
Study-Related Adverse Events (AEs)
Timeframe: During the Medial Branch Block procedure
Study-Related Adverse Events (AEs)
Timeframe: During the Lead Placement procedure (SOT)
Study-Related Adverse Events (AEs)
Timeframe: 1-week post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 2-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 3-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 4-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 5-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 6-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 7-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 8-weeks post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 3-months post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 6-months post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 9-months post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 12-months post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 18-months post-SOT
Study-Related Adverse Events (AEs)
Timeframe: 24-months post-SOT