Skip to content

Incidence of Adductor Canal Catheter Dislodgment

Positioning of Continuous Adductor Canal Catheters After Total Knee Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05961085
Enrollment
100
Registered
2023-07-27
Start date
2023-07-10
Completion date
2025-12-31
Last updated
2025-09-12

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

Conditions

Total Knee Arthroplasty

Brief summary

The goal of this observational study is to determine the incidence of dislodgement for adductor canal catheters after total knee arthroplasty on post-operative day 1. We will also attempt to identify factors associated with secondary catheter failure.

Detailed description

Total knee arthroplasty (TKA) is a common procedure for indications including osteoarthritis and malignancy involving the knee, with over 55,285 knee replacements performed between 2020-2021 in Canada. Ultrasound guided continuous adductor canal block (cACB) is the standard of care for postoperative analgesia for this procedure. The catheter is not always as effective at providing analgesia as would be expected - which could be due to displacement of the catheter. This displacement is most likely to occur peri-operatively or during physiotherapy post-operatively and as such, post-operative assessments can provide useful insight into causes of secondary failure. This prospective observational study aims to estimate the cACB dislodgment on POD 1 rate at a high volume, tertiary care referral centre, and identify factors associated with dislodgement and clinical sequelae. As this is an observational/QI study of the current standard of care at Sunnybrook Health Sciences Centre, anesthesiologists are free to use the cross sectional versus parallel insertion of the cACB per their discretion.

Interventions

Ultrasound guided Adductor Canal Catheter for total knee arthroplasty analgesia

Sponsors

Sunnybrook Health Sciences Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients scheduled for Total Knee Arthroplasty * Older than 50 years

Exclusion criteria

* Body Mass Index greater than 40 * Chronic opioid consumption (greater than 30mg oral morphine equivalent daily) * Contraindication to Adductor Canal Catheter

Design outcomes

Primary

MeasureTime frameDescription
Adductor Canal Catheter tip in correct position on postoperative day 1Postoperative day 1 (08:00AM)Ultrasound confirmation of injectate spread adjacent to the femoral artery on postoperative day 1 (08h00)

Secondary

MeasureTime frameDescription
Sensory blockPostoperative day 1 (08:00AM)Loss of sensation in the saphenous nerve distribution on postoperative day 1 (08h00)
Postoperative opioid consumption (08h00)Postoperative day 1 (08:00AM)Cumulative opioid consumption after total knee arthroplasty to postoperative day 1 (08h00)
Numeric Rating Scale for Pain (NRS) at rest on postoperative day 1 (08h00)Postoperative day 1 (08:00AM)Maximum pain score on 0-10 Likert Scale
Adductor Canal Catheter tip in correct position after insertionPreoperativeUltrasound confirmation of injectate spread adjacent to the femoral artery before surgery

Other

MeasureTime frameDescription
Patient satisfaction with analgesia on postoperative day 1Postoperative day 1 (08:00AM)Patient satisfaction measured by 0-10 Likert Scale
Adductor catheter occlusionPostoperative day 1 (08:00AM)Any recording of local anesthetic infusion pump recording an occlusion

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026