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Spots Global Cancer Trial Database for Contrast-Enhanced MRI for the Characterization of Ductal Carcinoma in Situ (DCIS)

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Trial Identification

Brief Title: Contrast-Enhanced MRI for the Characterization of Ductal Carcinoma in Situ (DCIS)

Official Title: Contrast-enhanced MRI for the Characterization of Ductal Carcinoma in Situ (DCIS)

Study ID: NCT00804128

Conditions

Breast Cancer

Study Description

Brief Summary: \*REFERRALS TO THIS TRIAL MUST BE THROUGH BREAST CARE CLINICIANS ONLY\* RATIONALE: Diagnostic procedures, such as contrast-enhanced MRI, may help find and diagnose ductal carcinoma in situ. PURPOSE: This study is to develop and refine magnetic resonance (MR) imaging methods for pre-operative staging of ductal carcinoma in situ, a pre-invasive form of breast cancer, and atypical ductal hyperplasia, a risk factor for developing cancer.

Detailed Description: OBJECTIVES: * Compare the DCIS optimized MRI to the standard clinical MRI. Using a scale of 1-5 from poor to excellent, images will be assessed for conspicuity of DCIS and atypical ductal hyperplasia (ADH) lesions, agreement of disease extent with biopsy, and overall image quality (artifact level, uniformity of fat suppression, contrast to noise ratio and signal to noise ratio). * Subjects with ADH, a benign condition that can also show enhancement on MRI, will be enrolled to explore the utility of the DCIS optimized MRI for distinguishing DCIS and ADH.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University of California, San Francisco, San Francisco, California, United States

Contact Details

Name: Nola M. Hylton, PhD

Affiliation: University of California, San Francisco

Role: PRINCIPAL_INVESTIGATOR

Name: Bonnie Joe, MD, PhD

Affiliation: University of California, San Francisco

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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