Clinical Trials Directory

Trials / Terminated

TerminatedNCT01391039

Diagnostic Study of Early Breast Cancer Using Ultrasound

Microbubble Contrast Ultrasound and Transient Elastography Imaging of Early Breast Cancer

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Sunnybrook Health Sciences Centre · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This is a pilot study designed to investigate new techniques to guide the appropriate diagnosis and treatment of Ductal Carcinoma In-situ (DCIS). The microvascularity and stiffness of the lesion may be prognostic factors that can guide the need for more or less extensive therapy or perhaps only imaging follow-up may be needed.

Detailed description

Women who have imaging findings suggestive of DCIS, who are having breast ultrasound and who are candidates for surgery will be eligible. They will receive a contrast-enhanced breast ultrasound after the intravenous injection of a microbubble contrast agent which will show the microvascularity. A subset of women will also have ultrasound elastography performed of the abnormality to evaluate its stiffness.

Conditions

Interventions

TypeNameDescription
DRUGPerflutren lipid microsphereIntravenous injection of 10 microL/kg once prior to ultrasound examination

Timeline

Start date
2011-09-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2011-07-11
Last updated
2015-11-30

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01391039. Inclusion in this directory is not an endorsement.