Qiu RB 2004.
Methods | Country: China Setting: hospital based Aim: to study the effects of Yanghuo Sanzi tang in the treatment of 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 60 postmenopausal osteoporosis patients enrolled: 30 in trial group, 30 in control group Inclusion criteria: diagnostic criteria for osteoporosis, BMD detected by DXA Exclusion criteria: not mentioned |
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Interventions | Experimental: Yanghuo Sanzi tang, 150 ml, twice a day, for 6 months Control: Caltrate, 2 tablets per day, for 6 months |
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Outcomes | BMD, E2, BGP, IL‐6 | |
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 | Low risk | The study appears to be free of other sources of bias |