RF TKA Prehabilitation
Knee Osteoarthritis
About this trial
This is an interventional prevention trial for Knee Osteoarthritis
Eligibility Criteria
Inclusion Criteria:
- Chronic knee pain, with Dynamic VAS ≥ 5
- Scheduled for elective total knee arthroplasty
- Functional impairment due to pain because of knee osteoarthritis
- Taking medications to control the pain.
- Ability to perform the 6 MWT.
Exclusion Criteria:
- ASA physical status > 3
- Morbid obesity (BMI >40)
- Revision of total knee arthroplasty
- Mayor neuropsychiatric disease
- Mayor cardiac, renal or hepatic failure
- Anemia (hematocrit <30%)
- Immunosuppression
- Rheumatoid arthritis
- Allergy to opioids, to local anesthetics or other medications used in the study,
- Chronic regular use of large doses of opioids (>20mg equivalent of morphine/day) or sedatives
- Unwillingness to have spinal anesthesia
- History of recent drug abuse
- Contraindication to receive regional anesthesia (e.g. coagulation defect)
- Inability to walk before the surgery
- Inability to perform physical tasks
- Contraindications to physical exercise and training
- Prior mayor knee surgery
- Connective tissue diseases affecting the knee
- Serious neurologic disorders
- Injection with steroids or hyaluronic acids during the previous 3 months
- Active sciatic pain
- Anticoagulant medications
Sites / Locations
- Montreal General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Radiofrequency group
Control (Sham Radiofrequency) group
In this group patients will receive in a sterile fashion continuous radiofrequency for 4 minutes to the 3 genicular nerves in the operative knee as well as Pulsed Radiofrequency at 42 degrees celsius, for 4 minutes (60-70 volts) to the saphenous nerve and the nerve to the Vastus Medialis, at the level of the adductor canal. The procedure is done under local anesthesia on an ambulatory basis. After the radiofrequency, Ropivacaine 0.5% 5 ml is injected to each one of the nerves, along with 5 milligrams of Methylprednisolone to each nerve. Once the procedure is completed (takes about 20 minutes), patients will be observed in the preoperative program facility for 30 minutes and then discharged home.
In this group patients will receive injections of the local anesthetic and steroids in the same anatomical locations, without activating the radiofrequency generator.