Adductor Canal Blocks With Bupivacaine and Magnesium After Same-day Discharge Total Knee Arthroplasty Improve Post-operative Pain Relief and Decrease Opioid Consumption: a Prospective Randomized Controlled Trial
Post-operative Pain, Acute
About this trial
This is an interventional supportive care trial for Post-operative Pain, Acute focused on measuring Same-day discharge total knee arthroplasty; Magnesium; Adductor canal block; Post-operative opioid consumption; Post-operative pain management
Eligibility Criteria
Inclusion Criteria:
- Patients undergoing unilateral primary total knee arthroplasty with spinal anesthetic and MAC followed by a unilateral adductor canal block with ultrasound guidance.
Exclusion Criteria:
- Patients on chronic anticoagulation upon admission
- Patients with significant genetic or acquired clotting/bleeding disorders (hemophilia, DIC, etc.) or significant platelet dysfunction
- Patients with prior back surgery or leg surgery that precludes spinal or regional anesthesia
- Infection at sites for regional/spinal anesthesia
- Allergy to local anesthetics
Sites / Locations
- St. Joseph Mercy Oakland Hospital
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
No_Mg
Mg
Ctrl Group. Post-operatively all patients will have an ultrasound-guided adductor canal block (ACB) with 30cc of 0.25% bupivacaine. Patients in this Arm (selected randomly) will not receive Mg (the intervention) in the block; instead they will receive 0.3mL of sterile saline.
Treatment Group. Post-operatively all patients will have an ultrasound-guided adductor canal block (ACB) with 30cc of 0.25% bupivacaine. Patients in this Arm (selected randomly) will receive 150 mg Mg (0.3 mL-the intervention) in the block.