Periprosthetic Fracture Registry (PPFx)
Multicenter Prospective Registry for Periprosthetic Fractures After Hip or Knee Arthroplasty
AO Innovation Translation Center
600 participants
Dec 31, 2018
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria8
- 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 Criteria2
- Pregnancy or women planning to conceive within the study period
- Prisoner
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Locations(13)
View Full Details on ClinicalTrials.gov
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NCT03378557