Cong 1995.
Methods | “Healthy antepartum cases were randomized and divided into 3 groups.” | |
Participants | Healthy primipara. Setting and dates of recruitment not stated (China) | |
Interventions | A: 120 mg calcium daily; B: 240 mg calcium daily; C: no calcium (D: 1 g calcium; E: 2 g calcium; E: no calcium: not included as trials with high risk of bias not included in high calcium dose review). | |
Outcomes | Biochemical studies; hypertension, pre‐eclampsia, birthweight, gestational age, method of delivery. | |
Notes | First period (low dose) April 1987 to June 1988 (groups A, B, C); second period (high dose) April 1989 to June 1990 (groups C, D, F). Similar results for groups A and B, which were combined in this meta‐analysis Source of funding: not stated. CoI: not stated. |
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not described |
Allocation concealment (selection bias) | Unclear risk | Not described |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No placebo |
Blinding of outcome assessment (detection bias) All outcomes | High risk | No placebo |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Loss to follow‐up not reported |
Selective reporting (reporting bias) | Unclear risk | Limited information |
Other bias | High risk | Very limited description of methods |