OPTIMISing induction of labour care: oral misoprostol versus balloon dilatation within a stratified inpatient to outpatient setting for pregnant woman with induction of labour [The OptiMis-IO study]

Womens' and Childrens' Service, Sunshine Coast Hospital and Health Service0 个研究点目标入组 280 人开始时间: 2024年8月14日最近更新: 2024年8月19日

试验速览

暂无简介。

•Live fetus, singleton pregnancy, cephalic presentation, planning a vaginal birth, labour initiated by induction of labour, intact membranes, normal cardiotocography, Modified Bishops Score less than 7 (or ARM not possible), 16 years or older, informed consent to participate (which includes a vaginal examination prior to induction of labour) and intention to follow recommended care. Participants who meet inclusion criteria who are from non-English speaking background and/or culturally diverse backgrounds will be offered interpreters and cultural support during recruitment and consent.

•Previous uterine surgery, major fetal congenital anomaly, suspected severe fetal growth restriction, decline to participate, planned caesarean section and non-English speakers without interpreter.

发起方

Womens' and Childrens' Service, Sunshine Coast Hospital and Health Service