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临床试验/NCT02660567
NCT02660567已完成不适用

The Impacts of Using Amr's Maneuver (Cervical Traction) on Atonic Postpartum Hemorrhage; Multi-centre Randomized Controlled Study

ClinAmygate1 个研究点 分布在 1 个国家目标入组 900 人开始时间: 2016年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
900
试验地点
1
主要终点
the incidence of postpartum hemorrhage

研究概览

简要总结

The impacts of using Amr's manoeuvre (cervical traction) on atonic postpartum hemorrhage is a randomized controlled, multi-centre study that aims to compare the incidence of post partum hemorrhage (PPH> 500 ml blood loss) within the first 24 hours of labor after using Amr's maneuver with active management of the third stage versus active management alone

详细描述

Primary:

Compare the incidence of post partum hemorrhage (PPH> 500 ml blood loss) within the first 24 hours of labor after using Amr's maneuver with active management of the third stage versus active management alone

Secondary:

Comparing:

  • The amount of blood loss in each arm of the study
  • Hematocrit before and after labor
  • Duration from delivery of placenta till discharge from the delivery room

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

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

入选标准

  • All pregnant females aged 18 years or more, candidate for normal vaginal delivery during the period of the study will be included

排除标准

  • Women presenting with pre-existing maternal hemorrhagic conditions such as factor 8 or 9 deficiency or Von Willebrand's disease or those who had assisted vaginal delivery

研究组 & 干预措施

Amr Maneuver

Experimental

Active management of third stage plus Amr's maneuver

干预措施: Amr maneuver (Procedure)

Active management alone

No Intervention

Active management of third stage alone

结局指标

主要结局

the incidence of postpartum hemorrhage

时间窗: 24 hour

the incidence of post partum hemorrhage (PPH\> 500 ml blood loss) within the first 24 hours of labor after using Amr's maneuver with active management of the third stage

次要结局

未报告次要终点

研究者

发起方
ClinAmygate
申办方类型
Other
责任方
Sponsor

研究点 (1)

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