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Clinical Trial Summary

The purpose of this study is to demonstrate the Sensitivity and Specificity of SonoVue®-enhanced ultrasound is superior to that of unenhanced ultrasound for the characterization of benign versus malignant FLLs using final diagnosis based on histology or combined imaging (CE-CT and/or CE MRI)/clinical data as truth standard.


Clinical Trial Description

Unit of analysis for the outcome measures was the lesion, equivalent to the subject, since each subject had a single lesion that was to be characterized. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00829413
Study type Interventional
Source Bracco Diagnostics, Inc
Contact
Status Completed
Phase Phase 3
Start date June 2010
Completion date July 2013

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