Actively Recruiting
High Risk Breast Clinic: Protocol for Women at Increased Risk for Developing Breast Cancer
Led by Carol Fabian, MD · Updated on 2025-10-29
3000
Participants Needed
1
Research Sites
2000 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
High Risk Breast Clinic: Protocol for Women at Increased Risk for Developing Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women with at least 2 times the normal risk of developing breast cancer
- Age between 30 and 65 years or within 10 years of the youngest age at diagnosis in a first degree relative
- More than six months since last use of antihormonal therapy
- More than one year since pregnancy, lactation, or chemotherapy
- Willing to have a mammogram within six months before fine needle aspiration
- Willing to stop taking NSAIDs or herbal supplements
- Willing to have blood drawn
You will not qualify if you...
- Presence of metastatic cancer of any kind
- Breast implants or tram flap breast reconstructions
- Radiation treatment to both breasts
- Current mammogram or clinical breast exam suspicious for cancer
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
B
Bruce Kimler, Ph.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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