SMART-KNEE External Validation Study: New Zealand
- Conditions
- Knee OsteoarthritisMusculoskeletal - Osteoarthritis
- Registration Number
- ACTRN12621001687886
- Lead Sponsor
- Dr Michael English
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
•Diagnosed with knee OA
•Imminently about to undergo primary unilateral TKA (by imminently, we mean is within 2 to 3 weeks of surgery including up to and on the day of surgery)
•Are willing and able to complete online PROMs tools
•Able to provide informed consent to participate
•Are available to be followed up for the duration of the study
•Source of knee symptoms is considered to be from any cause other than knee OA eg, rheumatoid arthritis, hip osteoarthritis, referred lower back pain, post traumatic arthritis, previous septic arthritis of the knee etc.
•Are undergoing bilateral TKA, revision TKA, unicondylar knee arthroplasty (UKA), or patellofemoral arthroplasty
•Significant bilateral knee symptoms
•Intra-articular injection in the affected knee within the last 3 months
•Patients younger than 45years
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method