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Clinical Trial Summary

Up to one hundred (100) female patients will be enrolled and consented to participate in the study. These women will be enrolled from screening assigned BIRADS 0, patient complaint, or referral for second opinion. The enrolled patient will accept CE-CBBCT scans within 4 weeks of her diagnostic mammography and before breast biopsy if biopsy is needed. The final diagnostic workup outcome of these enrolled patients needs to include at least 30 confirmed cancers cases.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03354611
Study type Interventional
Source Koning Corporation
Contact Avice O'Connell, MD
Phone 585-487-3308
Email avice_oconnell@urmc.rochester.edu
Status Not yet recruiting
Phase Phase 2/Phase 3
Start date August 2018
Completion date June 2019

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