Xiao W 2008.
Methods | Country: China Setting: hospital based Aim: to study the effects of Gusong decoction in the treatment of osteoporosis Study design: randomised controlled trial Analysis: T‐test Loss to follow‐up: not reported |
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Participants | Ethnicity: Chinese 40 osteoporosis patients enrolled: 20 in trial group, 20 in control group Inclusion criteria: Chinese diagnostic criteria for osteoporosis based on bone density levels Exclusion criteria: secondary osteoporosis |
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Interventions | Experimental: Gusong decoction (15 ml, 3 times a day) and alendronate sodium tablet (1 tablet per day), for 5 months Control: alendronate sodium tablet, 1 tablet per day, for 5 months |
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Outcomes | BMD, E2, ALP, IL‐6, BGP | |
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 | P value for the baseline comparison not stated |