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Clinical Trial Summary

Subjects with suspicious breast lesion (BIRADS category 4/5) who are scheduled to undergo biopsy will be recruited to undergo imaging evaluation with Contrast Enhanced Dual Energy Mammography (CEDM), Contrast Enhanced Breast MR (CEMR) and Contrast Enhanced Ultrasound (CEUS).


Clinical Trial Description

The co-primary endpoints are to estimate the sensitivity and specificity of CEUS relative to pathology determined diagnosis. 1. Positive predictive value of CEDM in detecting lesions seen on MR 2. Estimate the negative predictive value (TN/(TN+FN)) of CEUS as an adjunct. 3. Compare the frequency of recommendation of biopsy of MG±US vs MG±US plus CEUS as an adjunct based on BIRADS scores. 4. Comparison of background enhancement seen on CEUS with that seen on CEDM and CEMR. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03954015
Study type Interventional
Source Mayo Clinic
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Status Completed
Phase Early Phase 1
Start date October 15, 2019
Completion date October 5, 2021