Clinical Trials Directory

Trials / Unknown

UnknownNCT00248820

Contrast-Enhanced Ultrasound Ability in the Characterization of Ovarian Masses

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University Hospital, Tours · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study intends to assess the ability of contrast-enhanced ultrasound in the detection of benign and malignant ovarian masses compared to unenhanced ultrasound. By using an intravascular contrast agent, this noninvasive and feasible imaging technique will allow the investigators to define specific microcirculation patterns in 100 women with ovarian lesions. The intravascular contrast agent properties will be compared between benign and malignant adnexal masses. The final purpose of this ultrasonography is to allow the early detection of tumors and to improve the characterization between benign and malignant lesions.

Detailed description

SonoVue (Sulphur hexafluoride microbubbles) is a microbubbles preparation that is stable, resistant to pressure and specifically designed to be used as a contrast agent for ultrasound imaging. Study design : one contrast-enhanced ultrasonography is proposed before any surgery to patients with ovarian mass.

Conditions

Interventions

TypeNameDescription
PROCEDUREContrast-enhanced ultrasoundContrast enhanced ultrasound using Sonovue / 2.4 ml per injection - one or two injections (maximum of 9.6 ml).

Timeline

Start date
2002-09-01
Completion
2009-02-01
First posted
2005-11-04
Last updated
2007-11-22

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00248820. Inclusion in this directory is not an endorsement.