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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 40
Maximum Age: 69
Healthy Volunteers: t
View:

• • 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

Locations
United States
Virginia
UVA Breast Care Center
RECRUITING
Charlottesville
Contact Information
Primary
Kathy L Repich, RN
klr3b@virginia.edu
4342434540
Backup
Matthew M Miller, MD
MM5CA@hscmail.mcc.virginia.edu
Time Frame
Start Date: 2019-09-19
Estimated Completion Date: 2023-06
Participants
Target number of participants: 210
Treatments
Other: CESM Pre and Post Survey
Subject will be asked to complete a questionnaire that will ask you about your general attitude toward Contrast-Enhanced Spectral Mammography (CESM). Questions will include:~* Thoughts regarding risk of breast cancer~* Concerns regarding contrast procedures such as the CESM~* Past mammogram/breast imaging experience
Related Therapeutic Areas
Sponsors
Leads: University of Virginia

This content was sourced from clinicaltrials.gov