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Intra-Operative Adductor Canal Blocks

A Randomized Controlled Trial Assessing the Efficacy of Surgeon-performed, Intraoperative Adductor Canal Blocks in Same-Day Discharge Total Knee Arthroplasty

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05601427
Enrollment
200
Registered
2022-11-01
Start date
2023-03-22
Completion date
2025-12-28
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Knee Arthritis, Knee Osteoarthritis, Knee Pain Chronic

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).

Interventions

PROCEDUREaACB

The patient will undergo a pre-operative single-shot, ultrasound-guided ACB performed by an anaesthesiologist skilled in regional anaesthesia techniques. The ACB will be performed in a dedicated block room, immediately prior to administration of a spinal anaesthetic.

PROCEDUREsACB

The patient will undergo an intraoperative single-shot ACB performed by the treating surgeon following placement of the TKA components.

Sponsors

Ottawa Hospital Research Institute
Lead SponsorOTHER
Canadian Orthopaedic Foundation
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Patient Report PainUp to 24 hoursMean Numerical Pain Rating Scale (NPRS) scores on discharge
Pain medication useWhen spinal anesthesia resolves until 24 hours after surgerymorphine equivalents of pain medication

Secondary

MeasureTime frameDescription
Time to dischargeFrom PACU to dischargePost-operative time in minutes to discharge home
Admission to HospitalUp to 24 hours post-operativeFailure to discharge home requiring admission
Readmission RateUp to 24 hours post-operativeNumber of patients readmitted to the hospital within 24 hours
Timed Up and Go TestAt dischargeTime 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-operativeScore on the Quality of Recovery-15 questionnaire
Patient Reported Functionpre-operatively, at 2 weeks post-operativeDifference 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 Quality of Lifepre-operatively, at 2 weeks post-operativeDifference 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
Patient Reported Global Healthpre-operatively, at 2 weeks post-operativeDifference in scores on the PROMIS-10 - Global Health (questionnaire), which generates T-scores. Higher T-scores indicate better health.

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORSimon Garceau, MD

The Ottawa Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026