Comparison of Contrast Enhanced Mammography to Breast MRI in Screening Patients at Increased Risk for Breast Cancer
Completed · Not applicable
Conditions studied: Women at Increased Risk for Developing Breast Carcinoma
In brief
The purpose of this study is to determine if Contrast Enhanced Spectral Mammography (CESM) will be able to detect smaller/earlier breast cancers as well as breast MRI can.
Key facts
- Study ID
- NCT01716247
- Run by
- Memorial Sloan Kettering Cancer Center
- People needed
- 1000
- Starts
- 2012-10-01
- Expected to finish
- 2018-06-01
- Last updated by the study team
- 2018-06-19
Who can join
Age: 21 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women considered at increased risk for developing breast carcinoma (those with a lifetime risk of >15%due to family history, genetic predisposition, prior radiation therapy to the chest, prior biopsy showing a high risk lesion, or personal history of breast cancer) that are being screened with breast MRI.
- Women who have a screening digital mammogram on the day of CESM or within 365 days prior
You may not qualify if…
- Women under 21.
- Pregnant or possibly pregnant.
- Women who have a contraindication to the intravenous use of iodinated - contrast agent (i.e., allergy to iodinated contrastor severely impaired renal function with a creatinine level > or = to 1.3).
- Women with breast implants.
- Women with pacemakers.
- Women with aneurysm clips that don't allow for MRI.
- Women too claustrophobic to undergo MRI.
Where it is running
- Memorial Sloan Kettering Cancer Center — New York, New York, United States
Full record on ClinicalTrials.gov
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