Ye AN 1998.
Methods | Country: China Setting: outpatients and inpatients Aim: to observe the effects of Bushen Zhuanggutang in the treatment of senile osteoporosis Study design: randomised controlled trial Analysis: T‐test Loss to follow‐up: not reported |
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Participants | Ethnicity: Chinese 60 senile osteoporosis patients enrolled: 31 in trial group, 29 in control group Inclusion criteria: WHO diagnostic criteria for osteoporosis based on bone density levels, BMD detected by DXA Exclusion criteria: secondary osteoporosis |
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Interventions | Experimental: Bushen Zhuanggutang (1 dose per day, fried) and Caltrate (1 tablet per day), for 6 months Control: Caltrate (1 tablet per day), for 6 months |
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Outcomes | BMD | |
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 | No information provided |
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 | Unclear risk | No information on baseline |