Wang XD 2011.
Methods | Country: China Setting: hospital based Aim: to study the effects of Hugu capsule in the treatment of postmenopausal osteoporosis Study design: double‐blind, placebo‐controlled, randomised controlled trial Analysis: T‐test Loss to follow‐up: not reported |
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Participants | Ethnicity: Chinese 122 postmenopausal osteoporosis patients enrolled: 61 in trial group, 61 in control group Inclusion criteria: Chinese diagnostic criteria for osteoporosis Exclusion criteria: bone metabolic disease, endocrine disease, etc. |
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Interventions | Experimental: Hugu capsule (4 capsules, 3 times a day) and Caltrate (1 tablet per day), for 6 months Control: placebo capsule (4 capsules, 3 times a day) and Caltrate (1 tablet per day), for 6 months |
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Outcomes | BMD, 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 | Unclear risk | Patients were randomly allocated |
Allocation concealment | Unclear risk | No information provided |
Blinding All outcomes | Low risk | Double‐blind |
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 |