ACTRN12621001328864尚未招募未知
Effectiveness and safety of outpatient versus inpatient balloon cervical ripening preceding induction of labour
Madeleine Jones0 个研究点目标入组 3,672 人开始时间: 2021年9月29日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 3,672
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- o limit 至 o limit（—）
- 性别
- Female
入选标准
- •1. For health centres: to be currently performing inpatient cervical ripening with balloon catheters prior to induction of labour at term.
- •2. For individuals: All women undergoing induction of labour at or after 37 weeks of gestation with an unfavourable cervix requiring balloon cervical ripening (Bishop score < 7). Singleton pregnancy with no major fetal structurally abnormality, cephalic (head-first) presentation and intact membranes.
排除标准
- •Induction of labour before 37 weeks of gestation, major fetal structural abnormalities, intrauterine fetal death, multiple pregnancies, anomalous (non-cephalic) presentation, induction of labour without cervical ripening, utilisation of other pharmacological methods (prostaglandins) for cervical ripening when cervical ripening with balloon is contra-indicated or when the placement of the balloon is technically not possible, and necessity of hospital admission for other medical reasons prior to and during the balloon cervical ripening (in both phases).
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