Investigator Initiated Depuy Replacement knee In-Vivo Evaluation Study
Not Applicable
Completed
- Conditions
- OsteoarthritisMusculoskeletal Diseases
- Registration Number
- ISRCTN26541777
- Lead Sponsor
- niversity of Leeds (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
1. Patients (no age limit, either sex) with osteoarthritis of the knee undergoing unilateral knee replacement at Chapel Allerton Orthopaedic Centre
2. Patients with a functionally normal contralateral knee
Exclusion Criteria
1. Patients who cannot safely walk unaided
2. Patients who decline to give permission for their clinical data to be used in anonymised form for research purposes
3. Patients who are unable to give informed consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum knee flexion measured using the Fastrak electromagnetic motion tracking system (Polhemus, USA)
- Secondary Outcome Measures
Name Time Method A comparison of high performance activities (sit to stand and squatting) 12 months after surgery