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Contrast-enhanced Spectral Mammography (CESM) Breast Cancer Screening — S-CESM  

Mammography Clinical Trial

Official title:
Willingness of Women to Undergo a Contrast-enhanced Spectral Mammography (CESM) for Breast Cancer Screening and Their Experience Before and After CESM

Clinical Trial Summary

The purpose of this study is to evaluate how well women may adopt a Contrast-enhanced Spectral Mammography (CESM) as their yearly breast screening test compared to the standard 2-D or 3-D mammogram.

Clinical Trial Description

Contrast-enhanced spectral mammography (CESM) is an FDA approved tool for breast cancer detection. However, adoption into clinical practice has been slow. In this study, we will explore patient issues related to the use of CESM for breast cancer screening. For this study, 210 women with heterogeneous or dense breast tissue reported on a previous mammogram, will be recruited to undergo a screening Contrast-enhanced Spectral Mammography (CESM). The CESM will serve as the subject's annual screening breast exam for clinical care. A survey will be administered before and after the examination that evaluates the patient experience. Women will not be at high risk for breast cancer (<20% lifetime risk). All abnormal findings will be acted upon independently. Results of the general screening population survey will be compared with those of women who choose to undergo the CESM examination in order to evaluate the influence of age, education, and lifetime risk on decision making about advanced screening. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04904757
Study type Interventional
Source University of Virginia
Contact Kathy L Repich, RN
Phone 4342434540
Email klr3b@virginia.edu
Status Recruiting
Phase N/A
Start date September 19, 2019
Completion date June 2023
View Details
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