Treatment of Post-Operative Pain Following Orthopedic Surgery With SPRINT® Peripheral Nerve Stimulation (PNS) System
Lay Description
The purpose of this study is to determine if your knee pain changes when small amounts of electricity are delivered to the nerves in your leg by a device called the SPRINT PNS System (the study device).
Category
- Healthy Subjects Needed
- Mens Health
- Nervous System
- Reproductive Health
- Womens Health
- IRB Number
- 20210900HU
- NCT Number
- ct.gov registration not required
- Open to Enrollment
- Yes
Eligibility
- Eligible Ages
- 21 and over
- Eligible Genders
- All
- Accepts Healthy Volunteers
Inclusion Criteria
- At least 21 years old
- Underwent a primary unilateral total knee replacement procedure
- Knee pain directly resulting from Total Knee Replacement in affected knee
Exclusion Criteria
- Current high opioid use
- Body Mass Index (BMI) > 40 kg/m2
- Conditions with increased risk of infection
- Implanted electronic device
- History of bleeding or clotting disorder.
- Surgery on the affected knee since the primary Total Knee Replacement
- Uncontrolled Diabetes Mellitus Types I or II
- Pregnancy
Study Design
Arm Groups
Study Contact
Robert Villarreal
(210) 567-4527
villarrear10@uthscsa.edu
Robert Villarreal
(210) 567-4527
villarrear10@uthscsa.edu
Principal Investigator
Maxim Eckmann