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
| Type | Name | Description |
|---|---|---|
| DRUG | Perflutren lipid microsphere | Intravenous 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.