Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Washington University School of Medicine
With
National Institutes of Health (NIH)
Age
40–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Female.
Premenopausal (when menopausal status is uncertain, the investigators will measure follicle-stimulating hormone and estradiol to ascertain that a partcipant is premenopausal)
At least 40 years of age.
Dense breasts on routine mammogram (BI-RADS Category C and D)
Able to understand and willing to sign an IRB-approved written informed consent document.
You may not be if
History of breast or any other invasive cancer except for DCIS (ductal carcinoma in situ) who received only lumpectomy, LCIS (lobular carcinoma in situ), atypical hyperplasia, non-melanoma skin cancer, carcinoma in situ of the cervix.
Current use of tamoxifen, aromatase inhibitors, or bisphosphonates, or RANKL inhibitors
Concurrent participation in another cancer chemoprevention trial (unless no longer receiving the intervention).
Pregnant, lactating, or planning to get pregnant while the trial is ongoing.
Recent history of invasive dental procedure (e.g. tooth extraction, dental implant, oral surgery).
Unhealed and/or planned dental/oral surgery.
History of osteonecrosis/osteomyelitis of the jaw.
