| Methods |
"Randomized", but method not specified. |
| Participants |
80 women with singleton pregnancies and BS < 5. |
| Interventions |
Oral or vaginal misoprostol 50 mcg 6‐hourly (max 4 doses). |
| Outcomes |
Brief maternal and fetal outcomes. |
| Notes |
Short report only ‐ few details. |
| Risk of bias |
| Bias |
Authors' judgement |
Support for judgement |
| Random sequence generation (selection bias) |
Unclear risk |
Randomized", but method not specified. |
| Allocation concealment (selection bias) |
Unclear risk |
Method was not described. |
| Incomplete outcome data (attrition bias)
All outcomes |
Unclear risk |
Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |
| Selective reporting (reporting bias) |
Unclear risk |
Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |
| Other bias |
Unclear risk |
Insufficient information to permit judgement of ‘Low risk’ or ‘High risk’. |
| 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’. |
