The primary objective of this clinical trial is to determine the effects of hesperidin on biochemical markers of bone in post-menopausal women. The secondary objectives are: * To investigate changes in bone formation and bone resorption markers in response to hesperidin intake * To compare the efficacy of hesperidin in a milk versus biscuit * To collect safety information of hesperidin consumption in a human trial
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
144
250 mg of hesperidin twice a day taken oraly in a biscuit or in milk for 6 months
Hospital of UKM, National University of Malaysia
Kuala Lumpur, Malaysia
Percentage change from baseline for bone formation (serum P1NP & osteocalcin) and bone resorption (urinary NTX & serum CTX) markers
Time frame: Six months
Full blood biochemistry analyses including lipid profile
Time frame: 6 months
Percentage change from baseline for osteoarthritis markers (CTX2 and others)
Time frame: 6 months
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