Status:
COMPLETED
Assessment of Conventional and Patient-specific Instrumentation in Total Knee Arthroplasty
Lead Sponsor:
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Collaborating Sponsors:
Canadian Orthopaedic Foundation
Smith & Nephew, Inc.
Conditions:
Osteoarthritis
Eligibility:
All Genders
20-80 years
Phase:
NA
Brief Summary
This study will use a special type of x-ray called radiostereometric analysis (RSA) imaging to determine whether patient-specific instrumentation for total knee arthroplasty (replacement) has an effec...
Detailed Description
This is a prospective randomized controlled trial which will enroll 50 patients undergoing total knee replacement surgery. All study patients will undergo an MRI prior to surgery. Half (25)of these pa...
Eligibility Criteria
Inclusion
- Undergoing primary total knee replacement surgery
- No previous knee hardware (ie.Uni-Knees, or high tibial osteotomy)
- BMI \< 40
- Study patients should live within 100 km of our facility to ensure availability for follow-up
Exclusion
- Pregnancy or considering pregnancy
- BMI \> 40
- Unable to undergo MRI screening
Key Trial Info
Start Date :
June 1 2015
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2018
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT02230215
Start Date
June 1 2015
End Date
August 1 2018
Last Update
November 8 2018
Active Locations (1)
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1
University Hospital
London, Ontario, Canada, N6A5A5