High Risk Breast Clinic: Protocol for Women at Increased Risk for Developing Breast Cancer

Recruiting now

Conditions studied: Breast Cancer

In brief

The overall goal of this project is to develop an integrative system of breast cancer risk assessment based on epidemiologic and biologic risk variables, as well as to develop or refine risk biomarkers which may be useful in predicting and monitoring response to prevention interventions.

Key facts

Study ID

NCT00291096

Run by

Carol Fabian, MD

People needed

3000

Starts

1989-08-01

Expected to finish

2027-12-01

Last updated by the study team

2025-10-29

Who can join

Age: 30 and older, up to 65. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• women with at least 2 times the normal risk of developing breast cancer
• between the ages of 30-65 (or within 10 years of youngest age at diagnosis in first degree relative)
• greater than six months from ingestion of antihormonal therapy
• greater than 1 year from pregnancy, lactation, or chemotherapy
• willing to have a mammogram within six months prior to RPFNA
• willing to discontinue NSAIDS or herbal supplements
• willing to have blood drawn

You may not qualify if…

• no metastatic malignancy of any kind
• no breast implants or tram flap reconstructions
• no radiation to both breasts
• no women who have a current mammogram or clinical breast exam suspicious for cancer

Where it is running

• University of Kansas Medical Center — Kansas City, Kansas, United States (enrolling)

Full record on ClinicalTrials.gov

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