Chen X 2008.
Methods | Country: China Setting: hospital based Aim: to observe the therapeutic effect of Gukang decoction on primary osteoporosis Study design: randomised controlled trial Analysis: T‐test, Chi2test Loss to follow‐up: not reported |
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Participants | Ethnicity: China 83 primary osteoporosis patients enrolled: 42 in trial group, 41 in control group Inclusion criteria: Chinese diagnostic criteria for osteoporosis, BMD detected by DXA Exclusion criteria: not mentioned |
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Interventions | Experimental: Gukang decoction, 1 dose per day, for 4 months Control: alendronate sodium tablets, 10 mg, once a day, for 4 months |
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Outcomes | BMD, E2, adverse effects | |
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 | High risk | Sequence generated by some rule based on clinic time |
Allocation concealment | High risk | Allocation based on clinic time |
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 |