Treatment of Post-Operative Pain Following Orthopedic Surgery With SPRINT® Peripheral Nerve Stimulation (PNS) System
Completed · Not applicable
Conditions studied: Postoperative Pain, Total Knee Replacement, Total Knee Arthroplasty, Partial Knee Replacement
In brief
The purpose of this study is to gather information about how knee pain changes when small amounts of electricity are delivered to the nerves in the leg. This study will involve the use of a Peripheral Nerve Stimulation (PNS) System that is made by SPR Therapeutics (the sponsor of the study). The SPRINT PNS System was cleared by the FDA for up to 60 days of use in the back and/or extremities for the management of acute and chronic pain.
Key facts
- Study ID
- NCT04341948
- Run by
- SPR Therapeutics, Inc.
- People needed
- 56
- Starts
- 2020-08-06
- Expected to finish
- 2024-06-27
- Last updated by the study team
- 2025-08-27
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of Arkansas for Medical Sciences — Little Rock, Arkansas, United States
- University of California San Diego — San Diego, California, United States
- The Orthopaedic Institute — Gainesville, Florida, United States
- Better Health Clinical Research, Inc — Newnan, Georgia, United States
- NorthShore University HealthSystem — Evanston, Illinois, United States
- Ochsner Clinic Foundation — New Orleans, Louisiana, United States
- Ali K. Valimahomed MD PLLC — Holmdel, New Jersey, United States
- University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States
- Duke University — Durham, North Carolina, United States
- UT Health San Antonio — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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