Migration of the Restoris MultiCompartmental Knee Implant System in robotic-assisted unicompartmental knee arthroplasty: a 5 year follow up RSA study
Not yet recruiting
- Conditions
- degenerative joint diseaseOsteoarthritis1002321310005944
- Registration Number
- NL-OMON54033
- Lead Sponsor
- Reinier Haga Orthopedisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 33
Inclusion Criteria
- Indication for medial unicompartmental knee replacement mainly as a result of
moderately disabling joint disease because of: Painful osteo- or post-traumatic
arthitis or as an alternative to tibial osteotomy. - Patient qualified for UKP
based on physical exam and medical history - Patient is able to speak and write
Dutch - Patient is willing to participate and able to provide written informed
consent - Age > 18 years
Exclusion Criteria
- contraindication as described by the manufacturer
- patient has a known or suspected sensitivity or allergy to one or more
of the implant materials
- revision UKP surgery of the same compartment
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method