Su 1996.
Methods | "Randomised". Method unspecified. | |
Participants | 124 women with indication for induction of labour. Ages 20‐35; primigravid women with singleton pregnancies and cephalic presentation. | |
Interventions | Mifepristone 50 mg orally 12 hourly up a maximum dose of 200 mg. Control group women had no initial treatment, but were observed in hospital for 2 days. Women who were not in labour after 48 hours were given either oxytocin (50% either group) or vaginal prostaglandin (50% both groups). | |
Outcomes | Clinical, endocrine. | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |