Contrast-enhanced Spectral Mammography (CESM) Breast Cancer Screening

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40-69
SponsorUniversity of Virginia

About this trial

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.

Eligibility criteria

Qualifiers

• Female

40 to 69 years

Previous normal mammogram (BI-RADS 1 or 2) showing heterogeneous or extremely dense breast tissue within last 24 months

Scheduled for screening mammogram as part of the patient's clinical care

Disqualifiers

• No mammogram within last 24 months

Fatty or scattered fibroglandular tissue on last mammogram

History of allergy to iodinated contrast

History of renal disease or renal function abnormalities

Trial design

Treatments tested in this trial

  • Contrast-enhanced spectral mammography (CESM)

Treatment groups

210 Participants
are divided into 1 treatment group

Sponsors and collaborators