Cao W 2010.
Methods | Country: China Setting: hospital based Aim: to observe the therapeutic effect of integrated traditional Chinese and western medicine on postmenopausal osteoporosis Study design: randomised controlled trial Analysis: T‐test, Chi2 test Loss to follow‐up: not reported |
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Participants | Ethnicity: Chinese
120 postmenopausal osteoporosis patients enrolled: 60 in trial group, 60 in control group Inclusion criteria: WHO diagnostic criteria for osteoporosis based on bone density levels Exclusion criteria: serious women's illnesses, malignant tumour, diabetes, etc. |
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Interventions | Experimental: Chinese medicine (combinations of herbs) (1 dose per day, water fried 300 ml, twice a day), tamoxifen (20 mg per day) and Caltrate (600 mg, 1 to 2 tablets per day), for 3 months Control: tamoxifen (20 mg per day) and Caltrate (600 mg, 1 to 2 tablets per day), for 3 months |
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Outcomes | BMD, Ca, ALP, adverse events | |
Notes | No funding sources or declarations of interest for the primary researchers reported | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Adequate sequence generation | Unclear risk | Patients were randomly allocated |
Allocation concealment | Unclear risk | No information provided |
Blinding All outcomes | Unclear risk | Insufficient information to permit judgement of 'low risk' or 'high risk'. |
Incomplete outcome data addressed All outcomes | Low risk | No missing outcome data |
Free of selective reporting | Unclear risk | Not all the outcomes that were of interest in this review were reported |
Free of other bias | Low risk | The study appears to be free of other sources of bias |