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Evaluation of Intra-operative Ultrasound Contrast Enhancement in the Evaluation of Liver Tumors — Definity®  

Liver Tumors Clinical Trial

Official title:
Evaluation of Intra-operative Ultrasound Contrast Enhancement in the Evaluation of Liver Tumors

Clinical Trial Summary

The primary purpose of this study is to demonstrate the safety and effectiveness of using an intra-operative ultrasound contrast agent(Definity®) for the identification of known liver tumors.

Clinical Trial Description

The primary objective of this study is to demonstrate the safety of the use of intra-operative ultrasound contrast (Definity®) administration. The secondary objective of this study is to demonstrate the improved image quality and conspicuity of known liver tumors using contrast enhancement. ;

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00955097
Study type Interventional
Source University of Louisville
Contact
Status Terminated
Phase Phase 1
Start date May 2008
Completion date May 2010
View Details
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