Molecular Breast Imaging (MBI) in Patients With Suspected Ductal Carcinoma in Situ (DCIS)
| Status: | Completed |
|---|---|
| Conditions: | Breast Cancer, Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 25 - 90 |
| Updated: | 3/23/2017 |
| Start Date: | January 19, 2009 |
| End Date: | November 14, 2016 |
Evaluation of Molecular Breast Imaging in Patients With a High Likelihood of Ductal Carcinoma in Situ
In this research study, the investigators are testing a new type of breast camera, called
Molecular Breast Imaging, to see if it can find tumors in the subject's breast.
Molecular Breast Imaging, to see if it can find tumors in the subject's breast.
Patients who are suspected to have DCIS based on mammographic findings will be invited to
participate in this study. The investigators plan to recruit 200 patients who are scheduled
to undergo a breast biopsy for a breast lesion considered suggestive or highly suggestive of
DCIS as determined by a radiologist specializing in breast imaging. Each patient will have a
suspicious area of calcification on mammography of extent < 3 cm, or a non-focal area of
abnormality on ultrasound or MRI that is scheduled for evaluation by biopsy. Each patient
will undergo an MBI study immediately prior to biopsy. The study coordinator will approach
these patients and inform them of the research project. If they are interested in
participating, informed consent will be obtained and the patient will be scheduled for the
MBI study prior to the breast biopsy.
participate in this study. The investigators plan to recruit 200 patients who are scheduled
to undergo a breast biopsy for a breast lesion considered suggestive or highly suggestive of
DCIS as determined by a radiologist specializing in breast imaging. Each patient will have a
suspicious area of calcification on mammography of extent < 3 cm, or a non-focal area of
abnormality on ultrasound or MRI that is scheduled for evaluation by biopsy. Each patient
will undergo an MBI study immediately prior to biopsy. The study coordinator will approach
these patients and inform them of the research project. If they are interested in
participating, informed consent will be obtained and the patient will be scheduled for the
MBI study prior to the breast biopsy.
Inclusion Criteria:
- Women with a breast lesion suspicious for DCIS who are scheduled for a stereotactic
breast biopsy.
- Lesion must be considered suggestive or highly suggestive of malignancy according to
the Breast Imaging Reporting and Data System Atlas criteria (BIRADS 4 or 5).
- Women between 25 and 90 years of age.
Exclusion Criteria:
- Unable to understand or sign a consent form.
- Pregnant or lactating.
- Physically unable to sit upright and still for 30-40 minutes.
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