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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04670042
Study type Interventional
Source Stanford University
Contact
Status Withdrawn
Phase N/A
Start date June 25, 2021
Completion date May 2024

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