Prospective, monocenter post market clinical follow-up of a primary knee replacement bearing the CE-mark. 200 subjects will be recruited and followed up for up to ten years or until revision of the primary knee endoprosthesis, whichever occurs first. Documentation of clinical and radiological parameters within the clinical routine pre-operative and post-operative at 3 and 12 months and 2, 5 and 10 years to evaluate time to revision, pain situation, knee functionality, mobility and stability.
Study Type
OBSERVATIONAL
Enrollment
124
Landesklinikum Amstetten
Amstetten, Lower Austria, Austria
Time until revision
Time frame: 10 years
Improvement of clinical situation based on Knee Society Score
Time frame: 3 and 12 months, 2, 5, 10 years
Documentation of incidents
Time frame: Up to 10 Years
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