Investigation of the Effect of BONISTEIN(R) Bone Blend on Bone Mineral Density/Content and Biomarkers of Bone Health

This is an interventional prevention trial for Osteoporosis focused on measuring Soy Isoflavones, Bone Mineral Density, Bone Mineral Content, postmenopausal Women, Bone Markers, Bone Health, Phytoestrogens Read More

Inclusion Criteria:

• Female
• Age 45 (inclusive) to 55 years (inclusive)
• Race: Caucasian
• Non-smokers / Smokers up to 10 cigarettes/day
• Postmenopausal hormone status: 1-3 years since the last spontaneous menstrual bleeding and a follicle-stimulating hormone concentration (FSH) >75 IU/ml and 17-estradiol (E2) of < 20 ng/L
• Years since menopause between 1-3 years
• Natural menopause or total hysterectomy with bilateral salpingo-oophorectomy
• Subjects with E2 results within the inclusion criteria range will be assessed on an individual basis if FSH level is less than 75 IU/ml
• Assessed as age-related healthy, based on a pre-study examination including medical history, physical examination, ECG, vital signs and clinical laboratory. The examination will be performed by a MD at the study site within 1-2 months prior planned study start for the individual subject.
• Willingness and ability to give written informed consent and willingness and ability to understand, to participate and to comply with the study requirements.
• Ability to understand, speak, read and write the English language

Exclusion Criteria:

• T-score < -2.5 at total hip and spine (either or both)
• Suspect lack of compliance
• BMI > 30 or < 21
• Use of HRT within the previous 6 months
• Use of any drug which might interfere with bone-metabolism (bisphosphate, estrogen receptor modulators, calcitonin) within the previous 12 months
• Systematic practice of high intensity exercise
• Vegetarian nutrition or any other extreme dietary habits
• Use of dietary supplements while on study, except multi vitamin. No "wash out" period for supplements - must stop before run-in period and refrain until the end of the study.
• Participant in any other study or donation of blood during the last 30 days before start of each dosing phase (T0).
• Total genistein blood concentrations of > 100 ng/ml measured at pre-study examination
• Known hypersensitivity or allergy to soy, purified isoflavones, peanuts, fish, and/or genistein.
• Hepatitis screen (serology) positive or not performed
• Drug screen positive or not performed (at least amphetamines, benzodiazepines, cannabinoides, opiates).
• Subjects on a weight reduction program or a medically supervised diet
• Unexplained weight loss or weight gain of more than 5 kg in the three months prior to the study
• History of liver or pancreas diseases
• Cardiovascular diseases, even AV-block I0 (PQ time > 220 ms) and QTc time > 450 ms
• History of breast cancer, endometrial cancer and other malignancy except basal and squamous cell skin cancer
• History of thromboembolism or deep venous thrombosis
• Any fractures within one year except for fingers, toes and facial bones
• Subjects with susceptibility for fractures as a history of being a faller
• Endometrial thickness > 6 mm
• Endometrial polyps
• Untreated hypo- or hyperthyroidism
• Insulin-dependent diabetes mellitus, Crohn's Disease, Cushing Disease etc.
• Any condition which might interfere with absorption of the investigational product (e.g. malabsorption syndrome)
• Co-medication: Anticoagulants, parathyroid hormones, corticosteroids, thiazide diuretic
• Subjects who, during the previous 24 months, received a total fee payment greater than 5'000 USD for participation in biomedical research