| Methods |
randomisation not stated |
| Participants |
120 pregnant women, <56 days of amenorrhoea, Gynaecological Out‐Patient Department, Royal Infirmary Hospital, Edinburgh, Scotland |
| Interventions |
mifepristone 600mg (all)
group 1: gemeprost 0.5mg/pv after 48 hours
group 2: gemeprost 1mg/pv after 48 hours |
| Outcomes |
complete, incomplete abortion, onset and duration of bleeding,
side effects, haemoglobin levels |
| Notes |
1 woman received blood transfusion (group 2) |
| Risk of bias |
| Bias |
Authors' judgement |
Support for judgement |
| Allocation concealment (selection bias) |
Unclear risk |
B ‐ Unclear |
