The purpose of this study is to evaluate the Efficacy and the Safety of Monthly(RisenexM group) versus Weekly Oral risedronate(Risenexsplus group) in Korean postmenopausal osteoporotic women(Phase IV)
The purpose of this study is to evaluate the Efficacy and the Safety of Monthly(RisenexM group) versus Weekly Oral risedronate(Risenexsplus group) with Vitamin D in compliance, improvement of vitaminD and BMD in Korean postmenopausal osteoporotic women(Phase IV)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
196
once a month
once a week
Samsung Medical Center
Seoul, South Korea
The propotion of patients with 25(Oh)D level <20mg/ml of 12 months
Time frame: 1 year
The change of Bone Mineral Density(BMD) value
The change of Bone Mineral Density(BMD) value\[Time frame: 1 year\] The change of PTH(Parathyroid hormone value) \[Time frame:6months,1 year\] The change of Compliance - overall groups of Risenex plus vs Risenex M(2groups)
Time frame: 1year
The change of PTH(Parathyroid hormone value)
The change of Bone Mineral Density(BMD) value\[Time frame: 1 year\] The change of PTH(Parathyroid hormone value) \[Time frame:6months,1 year\] The change of Compliance - overall groups of Risenex plus vs Risenex M(2groups)
Time frame: 6months,1 year
The change of Compliance - overall groups of Risenex plus vs Risenex M
The change of Bone Mineral Density(BMD) value\[Time frame: 1 year\] The change of PTH(Parathyroid hormone value) \[Time frame:6months,1 year\] The change of Compliance - overall groups of Risenex plus vs Risenex M(2groups
Time frame: 1year
The change of 25(Oh)D level in patients.
Time frame: 6months,1year
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