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Intra-Operative Adductor Canal Blocks

O

Ottawa Hospital Research Institute

Status

Enrolling

Conditions

Knee Arthritis
Knee Pain Chronic
Knee Osteoarthritis
Anesthesia

Treatments

Procedure: sACB
Procedure: aACB

Study type

Interventional

Funder types

Other

Identifiers

NCT05601427
20220573-01H

Details and patient eligibility

About

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).

Enrollment

80 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Anesthesiologist-Performed Adductor Canal Block (aACB)
Active Comparator group
Description:
Patients will get a pre-operative adductor canal block performed by an anesthesiologist.
Treatment:
Procedure: aACB
Surgeon-Performed Adductor Canal Block (sACB)
Experimental group
Description:
Patients will get an intra-operative adductor canal block performed by the surgeon
Treatment:
Procedure: sACB

Trial contacts and locations

1

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Central trial contact

Sanjula Costa

Data sourced from clinicaltrials.gov

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