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

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.

Condition(s)Breast Carcinoma
StatusRecruiting
Study typeObservational
SummaryThis 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.
Who can participateInclusion 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 or CEM as part of a screening study are also eligible. 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) * Personal history of any other cancer (excluding in-situ, stage 0, and non-melanoma skin cancers and other pre-cancerous conditions) treated within the last 5 years.
Ages25 Years to 80 Years
SexFemale
Accepts healthy volunteersYes
Lead sponsorM.D. Anderson Cancer Center
LocationsHouston, Texas, United States
Start date2017-09-15
NCT IDNCT03408353
Official listinghttps://clinicaltrials.gov/study/NCT03408353

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