This registry supports international data collection and research on PPFx treatments after hip and knee arthroplasty.
A registry such as this ultimately aims to provide far-reaching benefits to society including reduced morbidity and mortality, improved patient safety, improved quality of care and medical decision-making, reduced medical spending, and advances in orthopaedic science.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age ≥18 years
* Post-operative PPFx after total or hemi hip or total or unicondylar knee arthroplasty (including the acetabulum, femur, patella and proximal tibia) requiring
* osteosynthesis alone or
* component revision plus plate/nail osteosynthesis
* Informed …
Inclusion Criteria:
* Age ≥18 years
* Post-operative PPFx after total or hemi hip or total or unicondylar knee arthroplasty (including the acetabulum, femur, patella and proximal tibia) requiring
* osteosynthesis alone or
* component revision plus plate/nail osteosynthesis
* Informed consent obtained, i.e.:
* Ability of the patient or assigned representative to understand the content of the patient information / Informed Consent Form
* Signed and dated EC / IRB approved written informed consent
* Ability to attend post-operative follow up visits
Exclusion Criteria:
* Pregnancy or women planning to conceive within the study period
* Prisoner
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