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Attune With TruMatch TM Personalized Solutions Instruments

UnknownNA

Sponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Conditions: Obesity, Osteoarthritis

Interventions: Attune TruMatch (TM) Patient-Specific Instrumentation

Countries: Canada

The purpose of our study is to determine, using a prospective, randomized-controlled trial, the economic viability and clinical outcomes associated with patient-specific instrumentation (PSI) for total knee arthroplasty in an obese patient population.

Eligibility overview

Sex: ALL

Age: 20 Years to 70 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* patients with body mass index (BMI; kg/m2) greater than 30 and less than or equal to 50
* Symptomatic knee osteoarthritis deemed most appropriately treated with total knee arthroplasty
* Patient greater than 19 and less than or equal to 70 years of age
* English-speaking

Exclusion Criteria:

* History of prior open knee surgery, infection, or previous knee trauma
* Simultaneous bilateral knee arthroplasty
* Underlying dementia, cognitive delay, any disorder, or geographic distance that would preclude the completion of the clinical questionnaires
* Inflammatory arthropathy
* Chronic pain syndrome
* Fibromyalgia

Locations (1)

London, Ontario, Canada