A prospective Randomized Single Blinded Clinical Study on TKA with and without Orthosensor
- Conditions
- knee prosthesesosteoarthritis10005944
- Registration Number
- NL-OMON40578
- Lead Sponsor
- Atrium Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 150
- Patients diagnosed with osteoarthritis and indicated for TKA
- Patients treated prospectively with the Vanguard Total Knee System
- Patients providing informed consent
- Age > 75 yrs
- BMI > 35
- Extreme varus valgus
- Patients who had a TKA on contra lateral side within the last 1 year
- Patients who will need lower limb joint replacement for another joint within one year
- Patients who require revision of previously implanted TKA
- Poor medical condition (e.g. patients with malignancy)
- Cognitive problems
- Language problems
- Patients diagnosed with rheumatoid arthritis, posttraumatic arthritis
- Not being eligible for being included due to any other medical conditions as decided by the ortopaedic surgeons of the Atrium MC
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method