跳至主要内容
临床试验/IRCT2016042627615N1
IRCT2016042627615N1已完成2 期

Clinical trial on the effectiveness of oxytocin and sublingual administration of misoprostol in premature rupture of membranes before the onset of the active phase of labor in term pregnancies

Vice Chancellor for Research, Mashhad University of Medical Sciences0 个研究点目标入组 86 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
86

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

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • Premature rupture of membranes after 37 weeks of gestation; not being in the active phase of labor; Bishop score below six; cephalic presentation (vertex); singleton pregnancy; no evidence of clinical or laboratory signs confirming chorioamnionitis before the intervention; confirmation of the normal status of the fetal heart.
  • Exclusion criteria: Prior history of uterine scar; placenta previa; unstable status of the fetal heart; non-cephalic presentation; sensitivity to misoprostol; history of glaucoma in misoprostol users; contraindication to vaginal delivery (e.g., narrow pelvis and genital herpes), and 8) parity = 5.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research, Mashhad University of Medical Sciences

相似试验