NCT00383032已完成不适用
Randomized Controlled Trial of Mifepristone Versus Laminaria for Cervical Ripening In Midtrimester Induction
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 72
- 试验地点
- 2
- 主要终点
- induction to delivery time
研究概览
简要总结
Data from other countries have suggested that oral mifepristone used as a cervical ripening agent may decrease induction to delivery time in midtrimester inductions. To our knowledge, there are no trials comparing mifepristone to laminaria in a standard clinical setting with standardized misoprostol induction protocol to examine the issue of induction to delivery time. We hypothesize that mifepristone will work at least as well as laminaria for midtrimester cervical ripening prior to induction of labor with misoprostol.
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
- None
入排标准
- 年龄范围
- 16 Years 至 —(Child, Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •pregnant women with fetal anomalies, aneuploidy, or demise at 15-22 weeks gestation
- •age greater than 16
- •able to speak English
排除标准
- •prior uterine scar or
- •allergy or history of bad reaction to any of the study drugs or
- •history of chronic adrenal failure or
- •porphyria or
- •concurrent long-term corticosteroid treatment
结局指标
主要结局
induction to delivery time
次要结局
- pain
- delivery within 24 hours
- need for post-partum D&C
- adverse events
研究者
研究点 (2)
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