CompletedNot Applicable

The RESET Clinical Trial: SPRINT® Peripheral Nerve Stimulation for the Treatment of Back Pain

United States230 participantsStarted 2020-06-17

Plain-language summary

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)

Who can participate

Age range

21 Years – 75 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Key Inclusion Criteria: * Chronic low back pain Key Exclusion Criteria: * Body Mass Index (BMI) \> 40 * Prior lumbar surgery * Implanted electronic device * Pregnant

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

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)

Trial details

NCT IDNCT04246281

SponsorSPR Therapeutics, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2026-04-27

View on ClinicalTrials.gov More Low Back Pain trials

Plain-language summary

Who can participate

Age range

21 Years – 75 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Key Inclusion Criteria: * Chronic low back pain Key Exclusion Criteria: * Body Mass Index (BMI) \> 40 * Prior lumbar surgery * Implanted electronic device * Pregnant

What they're measuring

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)