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A Randomized, Controlled, Multicenter Trial of Percutaneous Peripheral Nerve Stimulation (PNS) for the Treatment of Back Pain
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)
Age
21 - 75 years
Sex
ALL
Healthy Volunteers
No
University of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
IPM Medical Group
Walnut Creek, California, United States
Denver Back Pain Specialists
Greenwood Village, Colorado, United States
International Spine, Pain & Performance Center
Washington D.C., District of Columbia, United States
Emory University
Atlanta, Georgia, United States
Northwest Speciality Hospital
Post Falls, Idaho, United States
Millennium Pain Center
Bloomington, Illinois, United States
Sinai Hospital of Baltimore
Baltimore, Maryland, United States
Premier Pain Centers
Shrewsbury, New Jersey, United States
Duke University
Durham, North Carolina, United States
Start Date
June 17, 2020
Primary Completion Date
April 1, 2026
Completion Date
April 1, 2027
Last Updated
February 25, 2026
230
ACTUAL participants
SPRINT Peripheral Nerve Stimulation (PNS) System
DEVICE
Standard interventional management of low back pain
PROCEDURE
Lead Sponsor
SPR Therapeutics, Inc.
Collaborators
NCT06661850
NCT03836248
NCT07196709
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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