ACTRN12613000141741终止未知
In pregnant women, is the use of the Odon device during the second stage of labour feasible and safe for maternal and perinatal outcomes?
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 入组人数
- 130
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
- Non-randomised trial
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18 Years 至 35 Years（—）
- 性别
- Female
入选标准
- •Age more or equal to 18 years, and less or equal 35 years
- •- Singleton pregnancy
- •- Gestational age equal to or more than 37 weeks
- •- Live fetus
- •- Fully dilated cervix
- •- Membranes ruptured (spontaneous or artificial).
- •- Any anterior occiput presentation.
- •- Station level equivalent to 2 cm or more below the spines
- •- Fetal Heart Rate Pattern recorded by continuous fetal electronic monitoring meeting the following criteria: (i) stable baseline rate between 110 and 160 beats/min, (ii) normal short and long term variability, (iii) absence of late decelerations.
排除标准
- •- Suspected or confirmed maternal infection
- •- Prolonged rupture of membranes (>24 hours)
- •- Meconium stained
- •- History of coagulation disorder
- •- Previous uterine surgery
- •- Intrapartum hemorrhage
- •- Absolute cephalopelvic disproportion
- •- Known recto-vaginal Streptoccocus B Haemolyticcus positive culture
- •- Known HIV positive women
研究者
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