Using Peripheral Nerve Stimulation (PNS) to Treat Chronic Post-surgical Pain (CPSP) After Knee Surgery
WithdrawnNot applicableNCT04670042
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
SPRINT PNS System will be offered to patients with postoperative knee pain following primary unilateral total knee arthroplasty (TKA) who meet eligibility criteria and consistent with established coverage policy. SPRINT PNS System will be implanted for 60 days. At the discretion of the physician, the first lead may be placed to stimulate the nerve innervating the region of greatest pain. If pain is not adequately addressed by the first lead when assessed at 10 days, a second lead may be placed approximately 2 weeks following the initial lead placement.
Study details
- Official title
- Feasibility and Effectiveness of Using Peripheral Nerve Stimulation (PNS) to Treat Chronic Post-surgical Pain (CPSP) Following Total Knee Arthroplasty.
- Conditions
- Injury
- Nerve, Peripheral, Multiple
- Chronic Post-Procedural Pain
- Total Knee Arthroplasty
- Surgery
- Knee Injuries
- Knee Pain Chronic
- Postoperative Pain
- Chronic Postoperative Pain
- Interventions
- Device: SPRINT® Peripheral Nerve Stimulation (PNS) System (510k Cleared)
- Sponsor
- Stanford University
- Collaborators
- SPR Therapeutics, Inc.
- Start date
- 2021-06-25
- Primary completion
- 2022-08
- Sex
- All
- Age range
- from 21 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * At least 21 years old * Underwent a primary or revision unilateral TKA * Completed all CHOIR questionnaires before and after TKA surgery * Persistent postsurgical knee pain ≥ 5 of 10 during ambulation as demonstrated on the CHOIR assessment. * Must meet the definition of chronic pain. 1. Pain that continues or is expected to continue for longer than 3 months from its initial onset or 2. Persistent pain that at the discretion of the physician has not resolved within the normal time course of healing or 3. Pain requiring opioid use beyond 30 days. Exclusion Criteria: * Patients with a pre-operative history of moderate to high dose use of opioids (≥ 50 morphine milligram equivalents (MME) average per day) * Patients taking opioids for reasons other than pain in knee that underwent TKA * Patients with arthrofibrosis or indicated for manipulation under anesthesia * BMI \>35 * Uncontrolled Diabetes Mellitus Types I or II, indicated by an HbA1c \>7.0% within the last 3 months * Vulnerable population (e.g. pregnant women, prisoners, minors, or employees) * Deep brain stimulation (DBS) system, an implanted active cardiac implant, or any other implantable neurostimulator whose stimulus current pathway may overlap the SPRINT stimulator's current pathway. * Any other condition that may interfere with the ability to participate in a clinical trial (e.g., anatomy that may interfere with lead placement, nerve damage in affected leg, pain caused by knee implant requiring revision, compromised immune system) as determined by the Investigator * Workers Compensation
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04670042