Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:37 AM
Ignite Modification Date:
2025-12-25 @ 3:37 AM
NCT ID:
NCT00093002
Eligibility Criteria:
Inclusion Criteria:
* Postmenopausal women defined as women who have stopped having menstrual periods
* Written informed consent to participate in the trial
* Biopsy confirmation of invasive breast cancer
* Evidence of hormone sensitivity
* Willingness to undergo biopsies
Exclusion Criteria:
* Any previous treatment for breast cancer
* Unwillingness to stop taking any drug known to affect sex hormonal status or a patient in which it would be inappropriate to stop.
* Any severe concurrent condition that would preclude surgery or that would jeopardize compliance with the study, e.g., uncontrolled cardiac disease or uncontrolled diabetes mellitus
* The presence of more than one primary tumor
* History of hypersensitivity to castor oil
* History of known bleeding disorders
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00093002
Study Brief:
Protocol Section:
NCT00093002