Spot Compression Ultrasound Compared to Traditional Breast Ultrasound

Part of paid clinical trials in Durham, North Carolina.

Sponsor
Duke University
Study ID
NCT07471672
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Breast Mass

Eligibility Criteria

Sex
FEMALE
Age
30 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Targeted ultrasound in the grid — DIAGNOSTIC_TEST
    Patients will have a single spot tomosynthesis mammogram image performed with an open compression paddle and concurrent targeted ultrasound imaging of the breast tissue contained in the open mammogram paddle while the breast is in compression.

Study Details

The purpose of this study is to determine the efficacy of targeted breast ultrasound ("ultrasound in the grid") performed concurrently with diagnostic mammogram during breast compression with an open mammogram paddle in lesion detection when compared to standard diagnostic breast ultrasound. Open paddle spot tomosynthesis and ultrasound in the grid images will be compared to the standard of care, and outcome measures will include comparing accuracy of lesion detection with the new technique versus the standard of care and differences in time to acquire the images for the new technique versus the current standard of care. Radiologists will also review the different sets of images and give confidence scores of lesion correspondence between mammogram and ultrasound. This will be a pilot study of 25 patients to demonstrate proof of concept and is intended to lay the foundation for future funded research with a larger patient population.

Key Dates

Start date
Apr 6, 2026
Status verified
Mar 2026
Primary completion
Aug 1, 2026
Completion
Aug 1, 2026

Study Design

Enrollment
25 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: Spot Compression Ultrasound
    This arm includes all participants enrolled in the study who will receive the experimental imaging technique

Primary Outcome Measure

Number of breast masses detected [ Time Frame: Single visit, up to approximately one hour ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Duke University Cancer CenterDurhamNorth Carolina27710
Eun L Langman, MD
919-684-2711

Find similar trials in Durham, NC