Contrast-enhanced Mammography in Women With a Personal History of Breast Cancer and Dense Breast Tissue: Benefit?
Opening soon NCT06993246
Run by Jean Seely · for 50 to 69 · Women
What this study is about
This study aims to assess the effectiveness of Contrast-Enhanced Mammography (CEM)as an alternative to traditional ultrasound for breast cancer screening in women with dense breasts and a personal history of breast cancer. CEM combines standard mammography with a contrast agent to better detect tumors, particularly in women with dense tissue where traditional mammograms may miss signs of cancer. The study will compare CEM with ultrasound and MRI to determine its accuracy in detecting cancer, reduce wait times for screening, and provide a more affordable option than MRI. Women who participate will have their screening done in one visit, improving convenience and access. The study will track cancer detection rates, biopsy results, and patient satisfaction over two years to evaluate the benefits of CEM for early breast cancer detection.
Who can join (things the study team will check)
✅ You may be able to join if…
- Women presenting at Rose Ages Breast Health Center, who are currently waiting for supplemental screening Ultrasound, according to pre-established guidelines at TOH for supplemental screening.
- Women ages 50-69 years of age
- Those willing to participate in the study, sign an informed consent and undergo IV iodinated contrast injection
- Women with dense breasts (category C or D) and normal mammograms (BI-RADS 1 or 2)
- No evidence of renal disease
🚫 You may not be able to join if…
- Patients with renal insufficiency (reduced eGFR <20ml/min)
- Previous allergic reactions to Iodine-based contrast.
- Prior contrast allergy (CT contrast)
- Thyroid Disease
Where this trial is running
- The Ottawa Hospital, Ottawa, Ontario, Canada
Who to contact
Dr. Jean Seely Department of Radiology, Radiation Oncology, MD, FRCPC, MD, FRCPC · 613-737-8899 · jeseely@toh.ca
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06993246.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.