Placebo
DrugPlacebo, calcium 900mg/d, VitD200iu/d and exercise
NCT Number: NCT00860964
The purpose of this trial is to study the efficacy and safety of low dose of estradiol valerate in the prevention and treatment of postmenopausal osteoporosis.
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Notify Me40 year–60 year
Female
Interventional
Phase 4
Research purposes: To assess the Impact of hormone therapy on quality of life in early post-menopausal women; To assess the Impact of hormone therapy on cardiovascular system in early post-menopausal women; To assess the Impact of hormone therapy on cognitive function in early post-menopausal women; To assess the Impact of hormone therapy on osteoporosis in early post-menopausal women.
Study Design:
The clinical trial research was divided into 2 groups. Treatment group given estradiol valerate 1mg/d, periodic application of medroxyprogesterone 6mg/d for 10 days, calcium 900mg/d, VitD200iu/d and exercise(Brisk walking every day 2 times, continued for 10 minutes each time). Control group given placebo, calcium,VitD and exercise were same with treatment group.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All patients meet the criteria:
Menopausal transition meet the criteria:
Early postmenopause meet the criteria:
Exclusion criteria
Placebo, calcium 900mg/d, VitD200iu/d and exercise
estradiol valerate 1mg/d,medroxyprogesterone 6mg/d for 10 days,calcium 900mg/d, VitD200iu/d and exercise
Time frame: 60 months
Time frame: 60 months
Peking Union Medical College
Other
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