Periprosthetic Fracture Registry (PPFx)

Launched by AO INNOVATION TRANSLATION CENTER · Dec 19, 2017

Keywords

ClinConnect Summary

The Periprosthetic Fracture Registry (PPFx) is a clinical study that collects information about patients who have experienced fractures around their hip or knee joint replacements. The goal of this registry is to gather data that can help improve treatments for these fractures, enhance patient safety, and ultimately improve the overall quality of care for those who undergo hip or knee surgeries. By understanding the best ways to treat these injuries, the registry aims to reduce complications and healthcare costs while advancing orthopedic science.

To participate in the study, individuals must be at least 18 years old and have had a fracture after receiving total or partial hip or knee joint replacements. They should be able to understand the study information and provide consent to participate, as well as attend follow-up appointments after their surgery. However, pregnant women or those planning to become pregnant during the study, as well as prisoners, cannot take part. If eligible, participants can expect to contribute valuable information that may help improve treatment for others in the future.

Gender

ALL

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 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