SLCTR/2008/002暂停未知
A randomised controlled trial comparing intra-vaginal Misoprostol with trans-cervical Foley catheter for the pre-induction cervical ripening
适应症
试验速览
- 阶段
- 未知
- 状态
- 暂停
- 发起方
- one
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Consented women with singleton gestation in vertex presentation at greater than 28 weeks gestation with Bishop’s score less than 6
排除标准
- •Rupture of membranes antepartum bleeding •active genital herpes infection •fetal death •placenta praevia •previous induction or pre-induction agent during the pregnancy, and known allergy to misoprostol •Women with history of cesarean deliveries will not be excluded
研究者
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