NCT00393731已完成2 期
A Randomized, Control Trial for Preinduction Cervical Ripening
The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 540 人开始时间: 2004年1月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 540
- 试验地点
- 2
- 主要终点
- Vaginal Delivery rates
研究概览
简要总结
The goal of this study is to compare the vaginal delivery rates in women undergoing induction of labor with an unripe cervix between oxytocin induction alone and preinduction cervical ripening with prostaglandin El (misoprostol). Secondary goals are to measure and compare the time intervals to delivery between the two methods.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Single
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women that are hospitalized for induction of labor that have a Bishop's score <5
- •singleton gestation
- •cephalic presentation
- •24 weeks gestational age
排除标准
- •Prior uterine surgery
- •malpresentation
- •placenta previa or abruption
- •clinically suspected or diagnosed intra amniotic infection
- •genital HSV infection
- •multiple gestation
- •premature rupture of the membranes
- •active labor
- •maternal/fetal conditions that may preclude labor induction in the opinion of the investigators
结局指标
主要结局
Vaginal Delivery rates
次要结局
- Time interval to delivery
研究者
研究点 (2)
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