Breast Cancer Clinical Trial

Mammography, Early Detection Biomarkers, Risk Assessment, and Imaging Technologies, MERIT Study

Summary

This study collects mammogram images, blood samples, and clinical information from women undergoing routine screening mammograms. Creating a bank of blood samples and a database of clinical and risk information may be used in future research related to breast cancer, other cancers, and women's health.

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Full Description

PRIMARY OBJECTIVES:

I. To establish a longitudinal cohort (n=10,000) of women who undergo mammography screening with follow-up for at least five years for each study participant or until breast cancer diagnosis.

II. To create a repository of blood specimens from the cohort to use for biomarker discovery and validation.

III. To create a comprehensive integrated database of imaging, clinical data, health measurements, and questionnaire data on the study participants.

OUTLINE:

Participants complete questionnaires over 15-25 minutes about personal and family history of cancer, health status, breast cancer risk factors, diet, weight gain, and physical activity, and undergo collection of blood samples at baseline and then annually for 5 years. Participants also undergo standard of care mammography at baseline and then annually for 5 years.

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Eligibility Criteria

Inclusion Criteria:

Willingness to participate in the study and ability to provide informed consent
Willingness to complete a questionnaire and to provide a blood sample at the initial visit and at follow up annual visits
Undergoing a screening mammogram at participating sites. Subjects undergoing routine annual diagnostic mammograms are also eligible at the MD Anderson site

Exclusion Criteria:

Current or recent (within the prior 6 months) history of breast feeding
Personal history of breast cancer (ductal breast carcinoma in situ [DCIS] or invasive breast cancer)
Treatment of any other type of cancer within the past 5 years excluding in situ cervical and non-melanoma skin cancer

Study is for people with:

Breast Cancer

Estimated Enrollment:

10000

Study ID:

NCT03408353

Recruitment Status:

Recruiting

Sponsor:

M.D. Anderson Cancer Center

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There is 1 Location for this study

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M D Anderson Cancer Center
Houston Texas, 77030, United States More Info
Jessica W. Leung
Contact
713-745-4555
[email protected]
Jessica W. Leung
Principal Investigator

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Study is for people with:

Breast Cancer

Estimated Enrollment:

10000

Study ID:

NCT03408353

Recruitment Status:

Recruiting

Sponsor:


M.D. Anderson Cancer Center

How clear is this clinincal trial information?

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