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Periprosthetic Fractures of the Femur Treated by Osteosynthesis

Completed
Conditions
Periprosthetic Fracture of the Femur
Registration Number
NCT02854566
Lead Sponsor
Brugmann University Hospital
Brief Summary

Observational retrospective study on 36 consecutive patients having had surgery for a periprosthetic fracture of the femur between 2010 and 2015.

The goal of the study is to test whether osteosynthesis was a secure choice at a certain age and with any type of Vancouver fracture.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  • Consecutive patients having had surgery between 2010 and 2015 within the CHU Brugmann hospital for a periprosthetic fracture of the femur (osteosynthesis).
Exclusion Criteria
  • Death during surgery.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Body Mass IndexUp to 2-3 days before surgery (pre-surgery radiography)

Demographic data

SexUp to 2-3 days before surgery (pre-surgery radiography)

Demographic data

Femoral componentUp to 2-3 days before surgery (pre-surgery radiography)

Need for cement within the femur or not

Blood lossDuring surgery (up to 2 hours)

Blood loss during surgery

ASA scoreDuring surgery (up to 2 hours)

ASA score

Fracture healing10 months after surgery

Healing status of the fracture (healed/not healed)

AgeUp to 2-3 days before surgery (pre-surgery radiography)

Demographic data

Prosthesis typeUp to 2-3 days before surgery (pre-surgery radiography)

PTH (total hip prosthesis) or BHP (bipolar hip prosthesis)

Time between 1st surgery and fractureUp to 2-3 days before surgery (pre-surgery radiography)

Time between 1st surgery and fracture

Mortality rate10 months after surgery

Mortality rate (any causes)

Complications rate10 months after surgery

Total complications rate (local + systemic + implant)

Type of fractureUp to 2-3 days before surgery (pre-surgery radiography)

Type of fracture according to the Vancouver International Classification

Secondary Outcome Measures
NameTimeMethod
LateralityUp to 2-3 days before surgery (pre-surgery radiography)

Prosthesis on the right or on the left side

Trial Locations

Locations (1)

CHU Brugmann

🇧🇪

Brussels, Belgium

CHU Brugmann
🇧🇪Brussels, Belgium

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