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Clinical Trial Summary

The primary objective is to determine how accurately one can estimate the size of the index tumor on preoperative imaging in patients with known breast cancer, using pathology as a reference standard. The primary endpoint, which will be measured on CEDM,and CE-MRI, is the maximum diameter (mm) of the index tumor.


Clinical Trial Description

The primary objective is to determine how accurately one can estimate the size of the index tumor on preoperative imaging in patients with known breast cancer, using pathology as a reference standard. The primary endpoint, which will be measured on CEDM,and CE-MRI, is the maximum diameter (mm) of the index tumor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01970670
Study type Observational
Source Stanford University
Contact
Status Completed
Phase
Start date April 2015
Completion date August 18, 2017

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