Methods | RCT. No information on how randomisation was carried out. | |
Participants | 30 pregnant women with 4 or more moderate to severe episodes of heartburn per week | |
Interventions | Intervention group: calcium carbonate antacids and H2receptor antagonist (Ranitidine) Control group: calcium carbonate antacid and placebo. |
|
Outcomes | Heartburn intensity. | |
Notes | Relatively large numbers of eligible women withdrew (already had relief with antacids alone) before randomisation | |
Risk of bias | ||
Bias | Authors’ judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | No information provided. |
Allocation concealment (selection bias) | Unclear risk | No information provided. |
Blinding (performance bias and detection bias) Women |
Low risk | Placebo controlled study. |
Blinding (performance bias and detection bias) Clinical staff |
Low risk | Placebo controlled study. |
Blinding (performance bias and detection bias) Outcome assessors |
Unclear risk | Not stated. |
Incomplete outcome data (attrition bias) All outcomes |
Low risk | Data available for all women randomised. |