Saphenous Nerve Block Versus Femoral Nerve Block for Total Knee Arthroplasty
- Conditions
- Total Knee Arthroplasty
- Interventions
- Procedure: Control Group
- Registration Number
- NCT01333943
- Lead Sponsor
- Hospital for Special Surgery, New York
- Brief Summary
Currently, the regional anesthetic standard of care for total knee replacement surgery is combined spinal/epidural, with or without a femoral nerve block, or FNB. Lasting approximately 18 hours, the FNB works by numbing the femoral nerve (and its branches), which is the major nerve controlling the knee joint. The femoral nerve also provides movement and sensation. While this regional anesthetic technique offers significant postoperative pain relief, it is possible that it may cause muscle weakness and increase patients' recovery time. Hence there is a need for an alternative technique, one that may help minimize postoperative pain as effectively as the FNB, while not causing weakness of the quadriceps muscle.
The saphenous nerve, a branch of the femoral nerve, provides sensation to the knee. Thus it is hypothesized that by "blocking" or anesthetizing the saphenous nerve with local anesthetic closer to where it branches off, the area around and below the knee will feel numb. Yet unlike with the FNB, the quadriceps muscle itself will still be able to function.
Patients will be randomized to receive FNB or saphenous nerve block. Quadriceps strength will be tested using a dynamometer before surgery (baseline), 6-8 hours following anesthesia administration, and on postoperative days 1 and 2. It is hypothesized that patients who receive FNB will experience a 50% decrease in quadriceps strength compared to baseline.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 94
- All patients ages 18-90 undergoing primary unilateral total knee arthroplasty
- Planned use of neuraxial anesthesia
- Ability to follow study protocol
- American Society of Anesthesiology (ASA) Class 1-3
- Contraindication to a spinal or epidural anesthetic
- Chronic opioid use (defined as daily or almost daily use of opioids for >3 months)
- Hypersensitivity and/or allergy to local anesthetics
- Intraoperative use of any volatile anesthetic
- Patients with a pre-existing neuropathy on the operative limb
- Contraindication to a femoral nerve block or saphenous nerve block
- Allergy to any of the study medications
- Non-English speaking patients
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control Control Group Femoral Nerve Block
- Primary Outcome Measures
Name Time Method Quadriceps Muscle Strength 48 hours following administration of anesthesia. Measurements were made by a handheld dynamometer while patients perform isometric exercises. Results are presented in kilogram-force (kgF) units. One kgF is equal to 9.80665 N.
- Secondary Outcome Measures
Name Time Method Total Length of Hospital Stay Total length of hospital stay NRS Pain Scores at Rest Postoperative day 4. Patients rated pain on a scale of 0-10, with 0 representing no pain and 10 representing worst pain.
Total Opioid Usage Postoperative day 4. Opioid consumption data were collected and converted to oral morphine equivalents.
Patient Satisfaction With the Nerve Block. 24 hours following administration of anesthesia. Patient satisfaction was measured on a 0-10 scale (0=not satisfied; 10=very satisfied).
Incidence of Postoperative Complications. Postoperative day 4.
Trial Locations
- Locations (1)
Hospital for Special Surgery
🇺🇸New York, New York, United States