跳至主要内容
临床试验/NCT02952807
NCT02952807已完成2 期

Sequential Versus Concurrent Use of Vaginal Misoprostol Plus Foley Catheter for Induction of Labor

Zagazig University1 个研究点 分布在 1 个国家目标入组 160 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
160
试验地点
1
主要终点
induction delivery interval (time from starting induction to delivery)

研究概览

简要总结

to compare between sequential and concurrent use of vaginal misopristol plus foleys catheter for induction of labor

详细描述

two groups of patients who are eligible for labor induction were randomized to either sequential use of vaginal misopristol plus foleys catheter or concurrent use of vaginal misopristol plus foleys catheter.

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

  • Indication for labour induction Term pregnancy with alive fetus Bishop score less than five

排除标准

  • Age less than 18 years Previous uterine scar Nonvertex presentation Non-reassuring fetal status Fetal anomalies Fetal growth restriction Genital bleeding Tumors, malformations and/or ulcers of vulva, perineum or vagina

研究组 & 干预措施

sequential

Active Comparator

sequential use of vaginal misoprotol Plus Foley Catheter for Induction of Labor.

干预措施: Misoprostol (Drug)

sequential

Active Comparator

sequential use of vaginal misoprotol Plus Foley Catheter for Induction of Labor.

干预措施: Foley Catheter (Device)

Concurrent

Active Comparator

Concurrent Use of Vaginal misoprostol Plus Foley Catheter for Induction of Labor.

干预措施: Misoprostol (Drug)

Concurrent

Active Comparator

Concurrent Use of Vaginal misoprostol Plus Foley Catheter for Induction of Labor.

干预措施: Foley Catheter (Device)

结局指标

主要结局

induction delivery interval (time from starting induction to delivery)

时间窗: 48hours

safety issue

次要结局

  • Severe neonatal morbidity or perinatal death(28 days)
  • Cesarean section(72h)
  • Serious maternal morbidity or maternal death(42 days)
  • Need of oxytocin for augmentation of labour(48h)
  • Number of doses needed to bring on labour(48h)
  • Hyperstimulation syndrome(24h)
  • Failed induction (failure to elicit contraction after 72 hours)(72h)

研究者

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

IBRAHIM ABD ELGAFOR

assistant lecturer

Zagazig University

研究点 (1)

Loading locations...

相似试验