Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
80 participants
INTERVENTIONAL
2023-03-22
2026-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Anesthesiologist-Performed Adductor Canal Block (aACB)
Patients will get a pre-operative adductor canal block performed by an anesthesiologist.
aACB
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.
Surgeon-Performed Adductor Canal Block (sACB)
Patients will get an intra-operative adductor canal block performed by the surgeon
sACB
The patient will undergo an intraoperative single-shot ACB performed by the treating surgeon following placement of the TKA components.
Interventions
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aACB
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.
sACB
The patient will undergo an intraoperative single-shot ACB performed by the treating surgeon following placement of the TKA components.
Eligibility Criteria
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Inclusion Criteria
2. Primary TKA booked as SDD
3. Diagnosis of osteoarthritis
Exclusion Criteria
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
18 Years
ALL
No
Sponsors
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Canadian Orthopaedic Foundation
OTHER
Ottawa Hospital Research Institute
OTHER
Responsible Party
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Principal Investigators
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Simon Garceau, MD
Role: PRINCIPAL_INVESTIGATOR
The Ottawa Hospital
Locations
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The Ottawa Hospital
Ottawa, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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20220573-01H
Identifier Type: -
Identifier Source: org_study_id
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