Home › Distal Femoral Fractures › NCT05792189
Distal Femur Fx: ORIF(Open Reduction and Internal Fixation) vs DFR (Distal Femur Replacement Total Knee Arthroplasty)
Evaluation of the Management of Periprosthetic Distal Femur Fractures and Native Knee Distal Femur Fractures, Comparing Open Reduction Internal Fixation With Distal Femur Replacement, a Prospective Cohort Study
Who can join
Ages 55 to 100 · All sexes
Full eligibility criteria
Inclusion Criteria: * English speaking patients * 55 years or older with Su Type II or Su Type III periprosthetic femur fractures or OTA/OA 33C or 338/3 native knee distal femur fracturing requiring surgical intervention and are medically fit to undergo surgical intervention Exclusion Criteria: * Patients with an active total knee prosthetic infection * Patients unable to undergo surgical intervention * Patient with an open fracture * Non-English-speaking patients * Oncologic/pathologic fracture * Poly-trauma patient (or other associated major orthopaedic injuries)
About the study
Supracondylar femur periprosthetic fractures about a total knee arthroplasty (TKA) are a catastrophic and challenging complication of TKA and unfortunately are increasing in incidence. Fixation of these fractures can be challenging due to altered anatomy for the TKA and the presence of the metallic femoral component and have a relatively high complication rate. As a result, some surgeons elect to treat these fractures with a distal femur replacement total knee arthroplasty (DFR). The purpose of this study is to prospectively evaluate periprosthetic femur fractures treated with ORIF or DFR and compare various outcomes measures (Get up and go times, KOOS Jr score)
What is being tested
- Timed Up and Go Test on subjects with ORIF of distal femur fractures (other)
- Koos Jr assesment on subjects with ORIF of distal femur fractures (other)
- Timed Up and Go Test on subjects with DFR of distal femur fracture (other)
- Koos Jr assesment on subjects with DFR of distal femur fracture (other)
Sponsor: University of Florida · Participants: 100 · Started: Apr 12, 2023
Contact the study team
- Matthew Patrick, MD · Phone: 352-273-7188
- Dykes Viginia, DAT · Phone: 352-273-7343
Official record on ClinicalTrials.gov — NCT05792189
Locations in the U.S.
| Florida | UF & Shands Orthopaedics and Sports Medicine Institute, Gainesville |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.