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 @ 12:39 AM
Ignite Modification Date:
2025-12-25 @ 12:39 AM
NCT ID:
NCT00843167
Eligibility Criteria:
INCLUSION CRITERIA:
* Diagnostic mammogram
* English speaking
EXCLUSION CRITERIA:
* Pregnancy (as determined by urine human chorionic gonadotropin (hCG) test)
* No biopsy referral after diagnostic mammogram
* Patient reported breast feeding
* Significant active medical illness which in the opinion of the investigator would preclude protocol treatment
* History of or active liver disease or baseline total bilirubin greater than institutional upper limit of normal
* Patient reported allergy or sensitivity to cruciferous vegetables
* Use of oral antibiotics within three months prior to randomization
* Oral steroid therapy at enrollment
* Current therapy with valproate acid or SAHA
* Current use of nutrient supplements or herbal remedies containing sulforaphane and unwillingness or inability to quit 72 hours prior to randomization and for the duration of the trial
* Radiation for currently-diagnosed disease prior to or during study supplementation
* Chemotherapy for currently-diagnosed disease prior to or during study supplementation
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
21 Years
Maximum Age:
120 Years
Study:
NCT00843167
Study Brief:
Protocol Section:
NCT00843167