ACTRN12612001184864尚未招募未知
In low risk pregnant women undertaking cervical priming for induction of labour, where there is no evidence of maternal or fetal compromise, will outpatient management, in comparison to inpatient management, result in comparable clinical outcomes, interventions, maternal satisfaction and complications?
Dr Chris Wilkinson0 个研究点目标入组 100 人开始时间: 2012年11月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Pregnancy is at term (37 completed weeks to 42 completed weeks. Intact membranes. Induction being performed for post-dates or social reason. Singleton, appropriately grown by clinical exam, cephalic presentation. (Clinical suspicion of growth restriction investigated by ultrasound assessment). -Cervical ripening for reasons other than fetal or maternal compromise.
排除标准
- •Known intra uterine growth restriction (< 10th percentile for gestational age), suspected intra uterine growth restriction, Gestational Hypertension and Pre-Eclampsia.*Conditions specific to catheter priming including: placenta previa, low placenta, unDx vaginal bleeding, known latex allergy, active vaginal infection, active genital herpes.
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