Actively Recruiting
Pre-Op THA Modelling
Led by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Updated on 2025-05-13
80
Participants Needed
1
Research Sites
173 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Replacing diseased hip joints with prosthetic implants in a procedure called total hip arthroplasty (THA) is associated with high rates of patient satisfaction, pain relief, and functional improvement when the implant is appropriately placed. Incorrect implant size or placement may lead to a breadth of negative outcomes, which could result in the need for implant revision. It is difficult to assess the precise orientation of patient hips on the operating table, with one study revealing that only 26% of acetabular cups placed without technological assistance are correctly positioned. Using computer navigation as a guide to achieve optimal implant alignment may improve successful placement rates. The additional incorporation of real-time modeling software may further help realize higher rates of successful implant placement. This study, therefore, aims to investigate a computer navigation system coupled with real-time modeling software to establish the benefit of such technology in the operating room, and further improve positive patient outcomes following THA. We hypothesize that including technological assistance in THAs will yield better patient outcomes compared to surgeries performed freehand.
CONDITIONS
Official Title
Pre-Op THA Modelling
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Osteoarthritis of the hip requiring primary total hip arthroplasty
- 40 years of age or older
- Body mass index (BMI) less than 40 kg/m2
- Able to provide informed consent, willing and able to complete study assessments and follow instructions
You will not qualify if you...
- Prior surgery on the indicated hip involving insertion of hardware
- Prior surgery on the lower spine involving insertion of hardware
- Hip or spinal fixed deformities or inflammatory/ossification spine conditions (e.g., DISH, ankylosing spondylolisthesis)
- Limitations in range of motion of the opposite hip
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
London Health Sciences Centre
London, Ontario, Canada, N6A5A5
Actively Recruiting
Research Team
B
Brent Lanting
CONTACT
L
Lyndsay Somerville
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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