Clinical Trials Directory

Trials / Unknown

UnknownNCT00859378

Cemented vs Non-cemented Semiendoprosthesis in the Treatment of Proximal Femoral Fractures

A Prospective, Randomized Study Comparing Cemented and Non-cemented Semiendoprostheses in the Treatment of Proximal Femoral Fractures in the Elderly Patients

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
Kuopio University Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The hip semiendoprosthesis is an acceptable method to treat the proximal femoral fractures. Traditionally, the cemented version of the semiendoprosthesis has been used for this indication. However, the cementing carries a risk of fat embolism during the pressurization of the cement. The fat embolism can be avoided when using the non-cemented semiendoprosthesis. In this study we want to find out whether there are any differences in the treatment results between the cemented and non-cemented semiendoprostheses when treating the proximal femoral fractures.

Conditions

Interventions

TypeNameDescription
DEVICECemented semiendoprosthesisApplication of a cemented semiendoprosthesis (Basis, Smith \& Nephew)
DEVICEnon-cementedPatients are treated with a non-cemented semiendoprosthesis (Biomet Taperloc, Biomet Inc.)

Timeline

Start date
2008-10-01
Primary completion
2014-12-01
Completion
2015-12-01
First posted
2009-03-11
Last updated
2015-04-07

Locations

2 sites across 1 country: Finland

Source: ClinicalTrials.gov record NCT00859378. Inclusion in this directory is not an endorsement.