Breast Cancer Clinical Trial
Study of Dual-energy (DE) Contrast-enhanced (CE) Digital Mammography
Summary
This is a feasibility study to evaluate dual-energy (DE) contrast-enhanced (CE) digital mammography to detect breast cancer in patients with increased breast density (BI-RADS category c or d). Eligible patients will be invited to have full-field digital mammography and dual-energy (DE) contrast-enhanced (CE) digital mammography to compare accuracy of the imaging methods for the detection of breast cancer.
Full Description
This is a feasibility study to evaluate dual-energy (DE) contrast-enhanced (CE) digital mammography to detect breast cancer in patients with increased breast density (Breast Imaging-Reporting And Data System category c or d). Eligible patients will be invited to have full-field digital mammography and dual-energy (DE) contrast-enhanced (CE) digital mammography to compare accuracy of the imaging methods for the detection of breast cancer
Eligibility Criteria
Inclusion Criteria:
Signed informed consent
At least 19 years old
Glomerular filtration rate> 60
Heterogeneously or extremely dense breasts (BI-RADS category c or d).
Exclusion Criteria:
History of iodinated contrast allergy
Pregnant or lactating as determined by routine standard practice
Personal history of breast cancer
History of prior breast excisional biopsy (Patients with a history of core needle biopsy will not be excluded)
History of prior breast reduction mammoplasty surgery
History of prior breast augmentation surgery
Mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study.
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There is 1 Location for this study
Birmingham Alabama, 35294, United States
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