Intra-Operative Adductor Canal Blocks
- Conditions
- Knee Pain ChronicKnee OsteoarthritisAnesthesiaKnee Arthritis
- Registration Number
- NCT05601427
- Lead Sponsor
- Ottawa Hospital Research Institute
- Brief Summary
Adductor canal blocks (ACB) have been recommended in total knee arthroplasty (TKA) to provide better control of post-operative pain, facilitate early ambulation, and reduce length of stay in the hospital. ACB is typically done before surgery by an anesthesiologist, which may increase time per case, cost, and requires the specialized skills of an anesthesiologist trained in regional anesthesia. Recent studies have suggested that surgeons can safely and reliably administer the adductor canal blocks (sACB) during surgery. However, there is currently very limited data on the clinical efficacy of such sACBs, and no studies assessing this technique in the context TKA that are discharged the same day. As such, this randomized control trial (RCT) is being done to compare sACBs to conventional anesthesiologist-performed adductor canal blocks (aACB).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 80
- Male and female patients aged 18 years or older
- Primary TKA booked as SDD
- Diagnosis of osteoarthritis
- Inability or refusal to sign informed consent form
- Non-English or French speaking, and no licensed translator, family member or substitute decision maker available.
- Non-osteoarthritis primary diagnosis
- Allergy to analgesic medications
- Contraindication to spinal and/or regional anaesthesia
- Any use of opioid pain medication within four weeks of the index procedure(13)
- Pain catastrophizing scale score ≥16 (8, 9, 14)
- History of cirrhosis
- History renal insufficiency
- History or sensory and/or motor neuropathy to the ipsilateral limb
- Simultaneous, bilateral TKA
- Non-TKA prosthesis
- Scheduled for non-SDD TKA.
- Preoperative varus/valgus of >10 degrees.
- Planned General Anaesthetic
- Use of Intrathecal Morphine
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Pain medication use When spinal anesthesia resolves until 24 hours after surgery morphine equivalents of pain medication
Patient Report Pain Up to 24 hours Mean Numerical Pain Rating Scale (NPRS) scores on discharge
- Secondary Outcome Measures
Name Time Method Timed Up and Go Test At discharge Time is takes, in seconds, to stand, walk 3m, turn around, walk back 3m, and sit back down
Patient Reported Quality of Recovery At 24 hours post-operative Score on the Quality of Recovery-15 questionnaire
Time to discharge From PACU to discharge Post-operative time in minutes to discharge home
Patient Reported Function pre-operatively, at 2 weeks post-operative Difference in scores on the Oxford knee score (questionnaire), rated from 0-48 with 48 being the best functional outcome and 0 being the worst
Patient Reported Global Health pre-operatively, at 2 weeks post-operative Difference in scores on the PROMIS-10 - Global Health (questionnaire), which generates T-scores. Higher T-scores indicate better health.
Readmission Rate Up to 24 hours post-operative Number of patients readmitted to the hospital within 24 hours
Patient Reported Quality of Life pre-operatively, at 2 weeks post-operative Difference in scores on the EQ-5D-5L questionnaire (Euro Quality of Life, 5 Dimension, 5 Level), rated from 11111 - 55555, with 11111 being full health and 55555 being worst health
Admission to Hospital Up to 24 hours post-operative Failure to discharge home requiring admission
Trial Locations
- Locations (1)
The Ottawa Hospital
🇨🇦Ottawa, Ontario, Canada
The Ottawa Hospital🇨🇦Ottawa, Ontario, CanadaSanjula CostaContact613-737-8899scosta@ohri.caSimon Garceau, MDPrincipal Investigator