Breast Cancer Clinical Trial

Comparison of Contrast Enhanced Mammography to Breast MRI in Screening Patients at Increased Risk for Breast Cancer

Summary

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.

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Eligibility Criteria

Inclusion Criteria:

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

Exclusion Criteria:

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.

Study is for people with:

Breast Cancer

Estimated Enrollment:

1000

Study ID:

NCT01716247

Recruitment Status:

Completed

Sponsor:

Memorial Sloan Kettering Cancer Center

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There is 1 Location for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

1000

Study ID:

NCT01716247

Recruitment Status:

Completed

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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