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临床试验/NCT02989324
NCT02989324已完成2 期

Low Dose Vaginal Misoprostol With or Without Foley Catheter for Late Second Trimester Pregnancy Termination in Women With Previous Multiple Cesarean Sections

Zagazig University1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
97
试验地点
1
主要终点
induction to expulsion interval

研究概览

简要总结

Vaginal Misoprostol Versus Combined Low Dose Misoprostol Plus Foley Catheter for Late Second Trimester Termination of Pregnancy With Previous Multiple Cesarean Sections

详细描述

this study aims to compare between Vaginal Misoprostol and Combined Low Dose Misoprostol Plus Foley Catheter for Late Second Trimester Termination of Pregnancy With Previous Multiple Cesarean Sections to assess safety and efficacy of theses methods.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • late second trimester
  • Previous Multiple Cesarean Sections

排除标准

  • Low lying placenta
  • allergy to misoprostol
  • patient refuse to participate

研究组 & 干预措施

Vaginal Misoprosto

Experimental

Vaginal Misoprosto for Late Second Trimester Termination of Pregnancy With Previous Multiple Cesarean Section

干预措施: MisoprostoL (Drug)

Misoprostol Plus Foley Catheter

Active Comparator

Misoprostol Plus Foley Catheter for Late Second Trimester Termination of Pregnancy With Previous Multiple Cesarean Sections

干预措施: MisoprostoL (Drug)

Misoprostol Plus Foley Catheter

Active Comparator

Misoprostol Plus Foley Catheter for Late Second Trimester Termination of Pregnancy With Previous Multiple Cesarean Sections

干预措施: Foley Catheter (Device)

结局指标

主要结局

induction to expulsion interval

时间窗: 24 hours

from time to start induction to time of complete expulsion of product of conception

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

IBRAHIM ABD ELGAFOR

assistant professor

Zagazig University

研究点 (1)

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