Khazardoost 2011 (V25).
Methods | Participants were "randomised". No other details available. | |
Participants | 60 women at term with intact membranes and BS < 6. | |
Interventions | A single dose of oral misoprostol 100 mcg or vaginal misoprostol 25 mcg | |
Outcomes | Delivery outcomes. Neonatal outcomes. Maternal side effect outcomes. |
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Notes | Data on oxytocin augmentation were excluded due to translation error. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Insufficient information about the sequence generation process to permit judgement of ‘Low risk’ or ‘High risk’. |
Allocation concealment (selection bias) | Unclear risk | B ‐ Unclear. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | The study did not address this outcome. |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |
Other bias | Unclear risk | Insufficient information to assess whether an important risk of bias exists. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |