Efficacy of a Temporary Peripheral Nerve Stimulation System in Patients with Osteoarthritis of the Knee
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Healthy Volunteers: f
View:
• Age of 21 and older
• Will receive a temporary PNS system for the management of chronic knee pain secondary to osteoarthritis
• Be capable of subjective evaluation, able to read and understand English-written questionnaires, and able to read, understand and sign the written informed consent in English
• Be willing and capable of giving informed consent
• Be willing and able to comply with study-related requirements, procedures, and scheduled visits
Locations
United States
Wisconsin
Aurora Health Center
RECRUITING
Fond Du Lac
Aurora Health Oshkosh
RECRUITING
Oshkosh
Contact Information
Primary
Mansoor M Aman, MD
mansoor.aman@aah.org
9204567715
Backup
Merve Buluk Figueira, MS
merve.figueira@aah.org
9204561551
Time Frame
Start Date: 2023-11-15
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 40
Treatments
Patients treated with a temporary PNS system
These patients will receive a temporary PNS system for their knee pain secondary to osteoarthritis
Related Therapeutic Areas
Sponsors
Leads: Wake Forest University Health Sciences