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临床试验/ACTRN12610000900011
ACTRN12610000900011尚未招募2 期

The effects of high versus low dose oxytocin on cesarean section rate, fetal and maternal outcomes for augmentation of labor in pregnant women gestational age > 37 weeks

Suppasiri Hayakungchat0 个研究点目标入组 300 人开始时间: 2010年10月25日最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
o limit 至 o limit(—)
性别
Female

入选标准

  • Mother criteria
  • 1. Singleton, gestational age 37 weeks or more
  • 2. Vertex presentation
  • 3. Bishop score = 9 or more
  • 4. Inadequate uterine contraction
  • Child criteria
  • 1. Viable fetus
  • 2. Singleton
  • 3. Vertex presentation
  • 4. well being fetus

排除标准

  • 1. Contraindication for augmentation of labor e.g. malposition, placenta previa, prior uterine scar, overdistended uterus, grand multiparity
  • 2. Cephalopelvic disproportion (CPD)
  • 3. Dead fetus in utero (DFIU)
  • 4. Contraindication in using oxytocin e.g. allergy to oxytocin, low blood pressure, fetal distress
  • 5. Medical complications: hypertension, HIV infection, coagulopathy, diabetes mellitus, heart diseases

研究者

发起方
Suppasiri Hayakungchat

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