Evaluation of Revaree Plus in Women With Breast Cancer
The purpose of this study is to find out whether Revaree Plus is effective at improving vaginal health for people who are having symptoms of vaginal dryness during breast cancer treatment.
• ≥18 years of age at the time of signing informed consent.
• Stage 0-3 hormone-receptor positive breast cancer confirmed at MSKCC
• Able to complete study questionnaires in English or Spanish
• Breast cancer patients must have completed chemotherapy or radiation therapy (and can be on maintenance therapy)
• Currently on an aromatase inhibitor or tamoxifen
• Currently have no clinical evidence of disease
• Reporting being bothered by vaginal symptoms of estrogen deprivation (i.e., vaginal dryness, dyspareunia, or discomfort \[pain with intercourse or examination\])
• A total score of 4 or greater in VAS
• Without history of other cancers (excluding non-melanoma skin cancer)
• Must sign an informed consent indicating that the participant understands the purpose of, and procedures required for the study and is willing to participate in the study