The purpose of the study is the evaluation of the clinical and radiological short- to long-term safety and performance of the aneXys cup. The data will be used for an ongoing evaluation of the product safety and performance.
Eligibility
Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria:
* Informed consent form (signed by participant and investigator)
* Primary implantation
* Suffer from primary or secondary osteoarthritis of the hip, femoral head and neck fractures or necrosis of the femoral head. In all cases a stable anchoring of the implant has to be possible.
* Age at inclusion: between 18 and 75 years old
* Willing to participate in the follow-up examinations
* Complete recovery is expected
Exclusion Criteria:
* Missing informed consent form (signed by participant and investigator)
* Known or suspected non-compliance (e.g. drug or alcohol abuse)
* Enrolment of the investigator, his/her family, employees and other dependent persons
* Patients younger 18 years old
* Revision surgery
* Presence of sepsis or malignant tumours
* ASA (American Society of Anesthesiologists) Classification \>3
* Pregnancy
Primary outcome measure(s)
Cup migration after 2 years — 2 years The primary endpoint will be the radiographic evaluation of the acetabular cup migration based on performed EBRA measurements 2 years after surgery.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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