Breast Cancer Clinical Trial
Official title:
Placebo-controlled Evaluation of the Homeopathic Drug BRN01 for the Treatment of Hot Flashes in Women With Non Metastatic Breast Cancer Treated by Adjuvant Hormonal Therapy
The purpose of this study is to evaluate the efficacy of a homeopathic treatment (BRN01) in reducing hot flash scores after 4 weeks of treatment.
Chemotherapy is used as an adjuvant treatment for breast cancer, like hormone therapy in
patients with hormone-sensitive breast cancer or immunotherapy in those with Human Epidermal
growth factor Receptor 2 (HER2)-overexpressing cancer.
These adjuvant treatments reduce the risk of recurrence and metastasis. The side effects of
hormone therapy are known and depend on the therapeutic strategy and the drugs used. The
side effects of Tamoxifen are similar to menopausal symptoms: hot flashes (half of the
female population), vaginal dryness or leukorrhea, nausea, irregular menstruation, benign
ovarian cyst and, less frequently, weight gain. Aromatase inhibitors have the same side
effects, though with lesser frequency and intensity. The incidence rate of hot flashes after
adjuvant treatment in menopausal women with localized breast cancer is 60 to 65 %, and these
reactions are very severe in one third of these women. Despite this fact, the management of
hot flashes is not systematic and there is currently no therapeutic strategy with proven
efficiency. BRN01 (Boiron laboratory) is a homeopathic remedy whose active ingredient is
already present in other homeopathic drugs indicated for the management of menopausal hot
flashes. BRN01 could reduce the intensity of the reaction in women with breast cancer
receiving adjuvant hormonal treatment.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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