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Clinical Trials/NCT02854566
NCT02854566
Completed
N/A

Periprosthetic Fractures of the Femur Treated by Osteosynthesis

Brugmann University Hospital1 site in 1 country36 target enrollmentJune 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Periprosthetic Fracture of the Femur
Sponsor
Brugmann University Hospital
Enrollment
36
Locations
1
Primary Endpoint
Mortality rate
Status
Completed
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
November 23, 2020
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tamas Illes

Head of clinic

Brugmann University Hospital

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Mortality rate

Time Frame: 10 months after surgery

Mortality rate (any causes)

Body Mass Index

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Demographic data

Sex

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Demographic data

Femoral component

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Need for cement within the femur or not

Blood loss

Time Frame: During surgery (up to 2 hours)

Blood loss during surgery

ASA score

Time Frame: During surgery (up to 2 hours)

ASA score

Fracture healing

Time Frame: 10 months after surgery

Healing status of the fracture (healed/not healed)

Age

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Demographic data

Type of fracture

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Type of fracture according to the Vancouver International Classification

Time between 1st surgery and fracture

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

Time between 1st surgery and fracture

Prosthesis type

Time Frame: Up to 2-3 days before surgery (pre-surgery radiography)

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

Complications rate

Time Frame: 10 months after surgery

Total complications rate (local + systemic + implant)

Secondary Outcomes

  • Laterality(Up to 2-3 days before surgery (pre-surgery radiography))

Study Sites (1)

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