Status:
ACTIVE_NOT_RECRUITING
Psychosocial Outcomes and Contralateral Prophylactic Mastectomy (CPM)
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborating Sponsors:
Patient-Centered Outcomes Research Institute
Conditions:
Breast Cancer
Eligibility:
All Genders
18+ years
Brief Summary
The goal of this research study is to learn more about how different treatment decisions may influence the quality of life in women with breast cancer. Researchers want to use what is learned from thi...
Detailed Description
With your verbal permission, you may have been asked to complete a questionnaire about your surgical treatment preferences for breast cancer as part of initial screening for this study. This takes abo...
Eligibility Criteria
Inclusion
- Newly diagnosed ductal carcinoma in situ (DCIS) or Stage I-III sporadic unilateral invasive breast cancer
- Age 18 or older
- Able to speak, read, and write English.
- Spouse/Partner: Married or living with patient for a year or more
- Spouse/Partner: Age 18 or older
- Spouse/Partner: Able to speak, read, and write English
Exclusion
- Patients with previous breast cancer
- Prior history of prophylactic mastectomy
- Known to have a germline gene mutation that predisposes them to an increased risk of breast cancer (e.g., BRCA1, BRCA2), and/or if they are considered at high risk for contralateral breast cancer on the basis of a strong family history of cancer
Key Trial Info
Start Date :
February 24 2014
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 30 2028
Estimated Enrollment :
345 Patients enrolled
Trial Details
Trial ID
NCT02263014
Start Date
February 24 2014
End Date
April 30 2028
Last Update
November 26 2025
Active Locations (2)
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1
Kelsey-Seybold
Houston, Texas, United States, 77030
2
University of Texas MD Anderson Cancer Center
Houston, Texas, United States, 77030