Pediatric Locking Nail for the Treatment of Femoral Fractures in Children

NCT00725894 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2017-06-21

No results posted yet for this study

Summary

The purpose of this multi-center prospective clinical outcomes study is to determine validity and safety of the pediatric locking nail for femoral fracture management in children with open physes.

Conditions

  • Femur Fracture

Interventions

DEVICE

Pediatric Locking Nail

The nail is pre contoured with a nine-degree anterior bow and is universal for right and left femoral.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Russell Schenck, PhD · Zimmer Biomet

Eligibility

Min Age
8 Years
Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2013-05-31
Completion
2013-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00725894 on ClinicalTrials.gov