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临床试验/TCTR20140515002
TCTR20140515002招募中3 期

Bilateral uterine compression to reduce blood loss and prevent postpartum haemorrhage after vaginal delivery

khalid abd aziz mohamed0 个研究点目标入组 320 人开始时间: 2014年5月15日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
320

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
20 Years 至 45 Years(—)
性别
Female

入选标准

  • Gestational age more than 28 weeks the gestational age was determined based upon the date of the first day of last normal menstrual period and confirmed by ultrasound scan during the 1st trimester
  • Women at high risk for primary atonic postpartum hemorrhage
  • Over distended uterus
  • Large fetus
  • Multiple fetuses
  • Distension with clots accidental hemorrhage
  • Exhausted myometrium
  • Prolonged labor
  • Oxytocin or prostaglandin stimulation
  • Chorioamnionitis
  • Previous uterine atony
  • Placenta previa
  • Marked anemia

排除标准

  • Postpartum hemorrhage
  • Retained placenta
  • Coagulopathy
  • Chronic medical illness hepatic renal
  • Pregnancy induced hypertension PIH
  • Refusal to participate in the study

研究者

发起方
khalid abd aziz mohamed

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