MedPath

Intra-Operative Adductor Canal Blocks

Not Applicable
Recruiting
Conditions
Knee Pain Chronic
Knee Osteoarthritis
Anesthesia
Knee 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
Inclusion Criteria
  1. Male and female patients aged 18 years or older
  2. Primary TKA booked as SDD
  3. Diagnosis of osteoarthritis
Exclusion Criteria
  1. Inability or refusal to sign informed consent form
  2. Non-English or French speaking, and no licensed translator, family member or substitute decision maker available.
  3. Non-osteoarthritis primary diagnosis
  4. Allergy to analgesic medications
  5. Contraindication to spinal and/or regional anaesthesia
  6. Any use of opioid pain medication within four weeks of the index procedure(13)
  7. Pain catastrophizing scale score ≥16 (8, 9, 14)
  8. History of cirrhosis
  9. History renal insufficiency
  10. History or sensory and/or motor neuropathy to the ipsilateral limb
  11. Simultaneous, bilateral TKA
  12. Non-TKA prosthesis
  13. Scheduled for non-SDD TKA.
  14. Preoperative varus/valgus of >10 degrees.
  15. Planned General Anaesthetic
  16. Use of Intrathecal Morphine

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pain medication useWhen spinal anesthesia resolves until 24 hours after surgery

morphine equivalents of pain medication

Patient Report PainUp to 24 hours

Mean Numerical Pain Rating Scale (NPRS) scores on discharge

Secondary Outcome Measures
NameTimeMethod
Timed Up and Go TestAt discharge

Time is takes, in seconds, to stand, walk 3m, turn around, walk back 3m, and sit back down

Patient Reported Quality of RecoveryAt 24 hours post-operative

Score on the Quality of Recovery-15 questionnaire

Time to dischargeFrom PACU to discharge

Post-operative time in minutes to discharge home

Patient Reported Functionpre-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 Healthpre-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 RateUp to 24 hours post-operative

Number of patients readmitted to the hospital within 24 hours

Patient Reported Quality of Lifepre-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 HospitalUp 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, Canada
Sanjula Costa
Contact
613-737-8899
scosta@ohri.ca
Simon Garceau, MD
Principal Investigator

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