Women At Risk: The High Risk Breast Cancer Program
Status unconfirmed
Conditions studied: Breast Cancer
In brief
The purpose of this study is to increase understanding of women who are at high risk for developing breast cancer. Data from this group will be collected and entered into a registry. This registry serves as a clinical database to support research in prevention, early detection and treatment of breast cancer.
Key facts
- Study ID
- NCT01034891
- Run by
- New York Presbyterian Hospital
- People needed
- 2000
- Starts
- 1991-01-01
- Last updated by the study team
- 2009-12-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- one or more first-degree relatives (mother, daughter, or sister) with pre-menopausal breast cancer
- two or more first-degree relatives with post-menopausal breast cancer
- tested positive for a BRCA1 or BRCA2 mutation
- a history of biopsy-proven atypical ductal hyperplasia or atypical lobular hyperplasia
- a history of biopsy-proven lobular neoplasia (lobular carcinoma in situ)
You may not qualify if…
- DCIS (ductal carcinoma in situ)
- previous diagnosis of breast cancer
Where it is running
- Women At Risk, Columbia University Medical Center — New York, New York, United States (enrolling)
- Women At Risk, Weill Cornell — New York, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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