Clinical Trials Directory

Trials / Completed

CompletedNCT00584402

Contrast Sonography for Evaluation of Liver Tumors Prior to Radiofrequency Ablation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the efficacy of the Definity (perflutren lipid microsphere Injectable Suspension) ultrasound contrast agent in identifying small tumors (hepatomas \& metastases) within the liver. Primary objective: To estimate the increase in conspicuity of small intrahepatic tumors with contrast-enhanced sonography Secondary Objectives: To estimate the effect of tumor type, size, location and depth on the conspicuity of small tumors on contrast-enhanced sonography

Detailed description

An estimated 75 patients (age 18 years of age or older) will be enrolled from the population of patients who present for ultrasound-guided radiofrequency ablation (RFA) of CT or MRI-confirmed multiple primary hepatocellular carcinoma (HCC) or metastatic carcinoma, with at least one of the tumors being ≤ 1.5 cm in diameter.

Conditions

Interventions

TypeNameDescription
DRUGperflutren lipid microspheresperflutren lipid microspheres IV in 0.1 cc doses, as needed, to enhance lesion conspicuity

Timeline

Start date
2007-04-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2008-01-02
Last updated
2017-07-11
Results posted
2017-07-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00584402. Inclusion in this directory is not an endorsement.