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Precision Supplemental Imaging in Women With Dense Breasts (PSID Trial)

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

Recent research has shown that, among women with extremely dense breasts and normal results on mammogram, magnetic resonance imaging (MRI) use has significantly reduced the occurrence of breast cancer that is diagnosed during the time between two regular screening mammograms (also known as interval cancers). The investigators have developed and validated an approach to use the whole mammogram image, develop a mammogram risk score (MRS), and calibrate this to the SEER breast cancer incidence rates for US women. This model (Prognosia Breast) generates an absolute 5-year risk of breast cancer and classifies approximately 5.7% of the population as high risk using the ASCO 3% cut point as used for endocrine therapy to reduce risk. Follow-up generates an incidence of 25.2 cases per 1,000 women per year.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 25
Maximum Age: 55
Healthy Volunteers: t
View:

• Normal screening mammogram within 90 days prior to enrollment. Bi-Rads of 1 or 2.

• Dense breasts, either:

‣ Class C density (the breasts are heterogeneously dense, which may obscure small masses)

⁃ Class D density (the breasts are extremely dense, which lowers the sensitivity of mammography)

• Assigned female at birth.

• Between 40 to 74 years of age (inclusive).

• Ability to understand and willingness to sign an IRB approved written informed consent document.

Locations
United States
Missouri
Washington University School of Medicine
RECRUITING
St Louis
Contact Information
Primary
Tabassum Ahmad, M.D.
ahmad.tabassum@wustl.edu
314-474-7696
Time Frame
Start Date: 2026-09-09
Estimated Completion Date: 2029-09-30
Participants
Target number of participants: 78
Treatments
Experimental: Feasibility: Recommended MRI
Consenting and eligible participants will be recommended to undergo MRI and will be followed to determine whether they complete the MRI.
Experimental: Arm A: Intervention - MRI + subsequent annual screening mammogram with MRI
Consenting and eligible participants will undergo an MRI and subsequent annual screening mammogram with MRI.
Active_comparator: Arm B: Regular Care - annual screening mammogram
Consenting and eligible participants will undergo annual screening mammogram per standard of care.
Related Therapeutic Areas
Sponsors
Leads: Washington University School of Medicine

This content was sourced from clinicaltrials.gov