The study is designed as a prospective, non-interventional multicentre cohort study. The product under Investigation will be used in Routine clinical practice and according to the authorized Instructions for Use (IfU). Aim of this observational study is to collect clinical and radiological results of the CoreHip® endoprosthesis system in a Standard Patient Population and when used in Routine clinical practice.
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Change of Hip Joint Function measured by Harris Hip Score over time (HHS)
Timeframe: Preoperative, 3 months postoperative, approx. 12-24 months postoperative and approx. 5 years postoperative