The purpose of this study is to learn if pain can be relieved by delivering small amounts of electricity (called "electrical stimulation") to the nerves at the top of the neck. This study will use a device called the SPRINT® PNS System. PNS stands for peripheral nerve stimulation (PNS). This device is cleared by the FDA for up to 60 days of use for relief of chronic or acute 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 and/or reduction in pain interference.
Timeframe: Up to 8-weeks after Start of Therapy (SOT)
Study-Related Adverse Events (AEs)
Timeframe: During the Lead Placement procedure (SOT)
Study-Related Adverse Events (AEs)
Timeframe: 24-48 hours post-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