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临床试验/ACTRN12615000546550
ACTRN12615000546550已完成3 期

Comparative study between carbetocin,oxytocin and misoprostol in prevention of postpartum hemorrhage following cesarean section in high risk cases.

Sherine Hosny Mohamed0 个研究点目标入组 240 人开始时间: 2015年5月28日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
240

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
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 35 Years(—)
性别
Female

入选标准

  • pregnant full term women that are scheduled to undergo ceserean section and have at least ONE of following (high risk patients for PPH) .
  • 1. Past history of PPH.
  • 2. Antepartum hemorrhage (eg placenta previa and accidental
  • hemorrhage.
  • 3. Over distension of the uterus (polyhydraminos, multiple pregnancy and macrosomia.
  • 4. Intra-amniotic infection.
  • 5. Uterine muscle exhaustion (prolonged labour and high parity).
  • 6. Anatomical uterine anomalies and uterine fibroid.

排除标准

  • Medical disorders with pregnancy eg hypertensive disorder, Diabetes Mellitus, serious cardiovascular disorders, migraine ,epilepsy, asthma etc…

研究者

发起方
Sherine Hosny Mohamed

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