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Temporary Peripheral Nerve Stimulation System for Osteoarthritis of the Knee

NCT06152029 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2025-11-06

No results posted yet for this study

Summary

The purpose of this study is to demonstrate the treatment outcomes of patients with chronic knee pain secondary to osteoarthritis that have received a temporary peripheral nerve stimulation system.

Conditions

Interventions

DEVICE

Temporary PNS system

This system remains in place up to 60 days, then removed.

Sponsors & Collaborators

  • Wake Forest University Health Sciences

    lead OTHER

Principal Investigators

  • Littlefield Lauren, MD · Aurora Medical Center Oshkosh - 855 N Westhaven Dr

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2025-10-20
Completion
2025-10-20

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06152029 on ClinicalTrials.gov