Clinical Trials Directory

Trials / Completed

CompletedNCT00175656

Titanium Elastic Nails in the Treatment of Pediatric Femur Fractures

Titanium Elastic Nails in the Treatment of Paediatric Femoral Fractures: A Prospective Randomized Clinical Trial of Eliminating Nail Protrusion to Decrease Soft Tissue Complications

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
4 Years – 15 Years
Healthy volunteers
Not accepted

Summary

Titanium elastic nails in the pediatric femoral fractures: A prospective randomized clinical trial of eliminating nail protrusion to decrease soft tissue complications

Detailed description

This study will be conducted as a prospective cohort study of children and adolescents treated with TEN for a femoral shaft fracture. All children and adolescents presenting to the Emergency department of a participating center with a femur fracture will be approached for inclusion in the study. The primary outcome for this study will be functional recovery, as measured using a pediatric specific generic QOL measurement tool. The clinical outcome measure which will be used will be the performance version of the ASK (ASK-p) which has been previously tested and shown to be valid, reliable, and responsive in children and adolescents with acute and chronic Orthopaedic disorders. The first time point for data collection will be at four months. Clinical data which will be obtained over the course of follow-up will include clinical evaluation of hip and knee range of motion, limb rotation, clinical measurement of limb length, fracture union, and the presence of complications, including the need for nail removal in the group in which it was not planned. The second time point for data collection will be at one year. Again, the ASK-p will be mailed to all subjects in advance to allow completion at the desired time. The return of questionnaires and process for reminder notifications will proceed in a similar fashion to the four month time point. Clinical and radiographic data will be collected in a similar fashion to the four month time point. No subjects will be excluded on the basis of failure to return questionnaires at the one year time point since this represents a secondary outcome.

Conditions

Interventions

TypeNameDescription
PROCEDUREElimination of titanium elastic nail prominence at the insertion site and leaving the nails in situSee Detailed Description.

Timeline

Start date
2007-01-01
Primary completion
2008-01-01
Completion
2008-01-01
First posted
2005-09-15
Last updated
2011-04-14

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00175656. Inclusion in this directory is not an endorsement.