The purpose of this study is to evaluate the effect of 20 mg of bazedoxifene in comparison to placebo on bone mineral density after 6 months of therapy in a population of postmenopausal Asian women.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
500
Unnamed facility
Beijing, China
Unnamed facility
Beijing, China
Unnamed facility
Nanjing, China
The percent change from baseline in lumbar spine bone mineral density (BMD) after 6 months of treatment
Additional BMD evaluation including total hip, femoral neck and trochanter at 6 months
Serum bone markers at 3 and 6 months
Lipid profile at 3 and 6 months
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Unnamed facility
Shanghai, China
Unnamed facility
Shanghai, China
Unnamed facility
Shanghai, China
Unnamed facility
Tianjin, China
Unnamed facility
Tianjin, China
Unnamed facility
Tianjin, China
Unnamed facility
Seoul, South Korea
...and 10 more locations