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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03562559
Other study ID # H17-02633
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 1, 2018
Est. completion date January 1, 2019

Study information

Verified date September 2019
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To control pain after total knee replacement surgery a catheter (tubing) is sometimes inserted into an anatomic space containing nerves that provide sensation to parts of the knee. This space is called the adductor canal.

The catheters often stop working before we remove them for unclear reasons. The investigators think this is because the catheters become dislodged from where it was meant to be. This could be due to repeated movements of the catheter tip brought on by patients contracting their leg muscles when they ambulate or perform physio.

The investigators want to confirm this by measuring the distance from a fixed spot on the patient's thigh to the adductor canal using an ultrasound machine. The leg will be measured in various positions to simulate muscle movements. A significant change in the distance could possibly contribute to catheter dislodgement and result in catheter failure.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 1, 2019
Est. primary completion date January 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients over or equal to the age of 18 years old who can understand the study protocol and are able to give consent

- Patients must be undergoing a primary total knee arthroplasty with neuraxial anaesthesia

Exclusion Criteria:

- Patients with an allergy to ultrasound transducer gel or measuring tape

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Measurements Using Ultrasound
Ultrasound measurements will be made in 5 positions. The ultrasound probe will be measuring from a fixed external location of the thigh. The 5 positions include: external rotation, neutral, manual tissue external rotation, straight leg raise at 30 degrees and hip/knee flexion at 90 degrees.

Locations

Country Name City State
Canada University of British Columbia Hospital Vancouver British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skin to Adductor Canal Distance Disparity The largest distance disparity as measured from the 5 different leg positions Measurements will be made on the day of surgery, no other assessment or follow up needed
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