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Evaluating Validity of Ultrasonography in Determining Distal Radius Fracture Reduction

Distal Radius Fracture Clinical Trial

Official title:
Study of Accuracy of Ultrasonography in Determining the Adequacy of Distal Radius Fracture Reduction

Clinical Trial Summary

The purpose of this study is to evaluate whether ultrasonography guidance compare with the simple radiography aids in determining the adequacy of distal radius fracture reduction.

Clinical Trial Description

Distal radius fracture is one of the most common causes for visiting the emergency department. Nowadays, simple radiography is used as a control standard for evaluating reduction of distal radius fractures. The disadvantages include time wasting, frequent x-ray exposures and use of more sedation in determining adequate reduction, made scientists to evaluate alternative method such as ultrasonography which fast, easy and less dangerous were considered as advantages. The investigators goal was to identify whether ultrasonography guidance compare with the simple radiography aids in determining the adequacy of distal radius fracture reduction. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01823692
Study type Interventional
Source Isfahan University of Medical Sciences
Contact
Status Completed
Phase Phase 2
Start date September 2011
Completion date September 2011
View Details
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