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| Methods | Stated to be double blind randomised trial. |
| Participants | Women 15 to 23 weeks' gestation undergoing termination for medical indications. |
| Interventions | Oral misoprostol (400 mcg 4‐hourly intervals) vs vaginal misoprostol (600 mcg 12‐hourly intervals). |
| Outcomes | Retained placenta, side effects. |
| Notes | Abstract available only; results presented as percentage only. |
