Prophylactic Infrapatellar Saphenous Neurectomy in Primary Total Knee Arthroplasty
- Conditions
- Knee Pain Chronic
- Interventions
- Procedure: Prophylactic Infrapatellar Saphenous Neurectomy in Primary Total Knee Arthroplasty
- Registration Number
- NCT04028947
- Lead Sponsor
- Mayo Clinic
- Brief Summary
Researchers are trying to determine if knee pain can be reduced by proactively protecting the free end of the saphenous nerve versus leaving it in the standard position during total knee arthroplasty.
- Detailed Description
Subjects scheduled for total knee arthroplasty will be randomized to two arms. One arm will have the standard saphenous nerve neurectomy during their surgery. The other arm will have the same neurectomy procedure with the free end of the nerve tucked into soft tissue to protect the nerve ending.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 178
- Primary unilateral total knee arthroplasty candidate
- Body Mass Index (BMI) >40
- Inflammatory arthritis
- Unable to follow up visits (long distance from Mayo Clinic)
- Poor compliance risk
- Health condition deemed by physician to preclude patient's ability to participate in the trial
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TKA with Neurectomy Prophylactic Infrapatellar Saphenous Neurectomy in Primary Total Knee Arthroplasty Subjects will the nerve excised and protected with soft tissue.
- Primary Outcome Measures
Name Time Method Pain after surgery 6 months Self-reported pain using Visual Analog Scale which is scored using a horizontal scale from 0-10cm with 10 being the worst pain.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Mayo Clinic in Florida
🇺🇸Jacksonville, Florida, United States