Lynne Cohen Consortium Project: Multi-Center Database/Registry

Completed

Conditions studied: Ovarian Cancer, Breast Cancer

In brief

Goals of this registry: 1.1 To collect and store very limited demographic information (age, birthdate, race and ethnicity), limited cancer risk and breast and ovarian disease history, as well as limited family history of breast and ovarian cancer on patients who are at risk of breast or ovarian cancer or who have had a diagnosis of either cancer, 1.2 To make available summary information (in an anonymous form) regarding the subjects in this registry to Consortium members, and other investigators, who can use these data to plan research projects and evaluate the feasibility of such projects, 1.3 To make available summary information (number of new patients seen in the clinic, number of mutations, number of preventive surgeries, average age of patients seen) to the Lynne Cohen Foundation for Ovarian Cancer Research, in order to document the numbers of subjects who utilize their supported clinics.

Key facts

Study ID

NCT00776958

Run by

M.D. Anderson Cancer Center

People needed

176

Starts

2008-07-01

Last updated by the study team

2014-07-31

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women who are 18 or older and meet one or more of the following criteria.
• Personal history of breast and/or ovarian cancer.
• Family history of breast and/or ovarian cancer (one or more relatives).
• Carrier of a mutation in the BRCA1 or BRCA 2 gene, or the presence of one of these mutations in a family member.

You may not qualify if…

• None

Where it is running

• University of Alabama, Birmingham/Department of OB/GYN — Birmingham, Alabama, United States
• USC/Norris Comprehensive Cancer Center — Los Angeles, California, United States
• NYU Cancer Institute — New York, New York, United States
• UT MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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