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Clinical Trial Summary

The purpose of this study is to determine whether the rate of fracture healing and fracture union, repaired with the LISS device, will be as good as or better than the usual fracture fixation systems.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00552331
Study type Interventional
Source Nova Scotia Health Authority
Contact
Status Completed
Phase Phase 4
Start date March 2003
Completion date July 2009

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