90
Participants
Start Date
February 2, 2022
Primary Completion Date
October 1, 2025
Study Completion Date
October 1, 2025
cRFA
cRFA intervention will occur under sterile conditions, the patient will be placed in a supine position on a table and a bolster to provide flexion in the treated knee joint. Skin and soft tissues will be anaesthetized with 2 mL 1% lidocaine at each of the three anatomic sites for cRFA, and a introducer needle will then be placed under ultrasound or fluoroscopic guidance to the SLG, SMG, and IMG nerves. Adjustments at these positions will be made when using ultrasound guidance in order to capture the geniculate nerve if the nerve and/or its accompanying vasculature can be directly visualized using greyscale or Doppler modes. When using ultrasound, the physician will note and record whether their positioning of the needle is based on bony landmarks, direct visualization of the nerve, and/or vascularity accompanying the nerve. Once the introducer needle is placed, the cRFA will be placed into the introducer needle.
RECRUITING
University of Rochester, Rochester
NOT_YET_RECRUITING
UC Davis Health, Sacramento
American Medical Society for Sports Medicine Collaborative Research Network
UNKNOWN
University of California, Davis
OTHER