Purpose

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.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
Study Type
Observational [Patient Registry]
Observational Model
Case-Only
Time Perspective
Prospective

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
William Obremskey, MD
William.Obremskey@vumc.org

More Details

Status
Recruiting
Sponsor
AO Innovation Translation Center

Study Contact

Cynthia Sob
+41 79 893 74 28
cynthia.sob@aofoundation.org

Detailed Description

To close the gap of missing clinical evidence regarding the treatment of periprosthetic fractures after arthroplasty of the hip or the knee with osteosynthesis. To drive further study hypotheses and to answer unforeseen questions. Main questions to be answered by the registry include (but are not exclusive) the following: 1. Influence of implants on outcome 2. Influence of surgical techniques on outcome 3. Influence of bone grafting on outcome 4. Identification of risk factors for failure 5. Identification of postoperative rehabilitation programs and its possible influence on the outcome 6. Influence of fracture type on outcome 7. To serve as a comparative dataset for future studies with improved implants and techniques

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.