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NovaLign Intramedullary Fixation System (IFS) for the Treatment of Humeral Fractures

Fracture Clinical Trial

Official title:
A Study to Evaluate the Safety and Effectiveness of the NovaLign Intramedullary Fixation System for the Treatment of Humeral Diaphysis Fractures

Clinical Trial Summary

This post-market clinical study is being done to evaluate the use of the NovaLign™ Intramedullary Fixation System in the treatment of humeral fractures.

Clinical Trial Description

This is an observational, prospective, nonrandomized open label, post-market clinical study, designed to evaluate the use a flexible intramedullary fixation device used in the treatment of fractures of the humerus. This is a multicentre trial. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00969839
Study type Interventional
Source NovaLign Orthopaedics, Inc
Contact
Status Recruiting
Phase Phase 4
Start date September 2009
Completion date March 2011
View Details
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