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临床试验/IRCT20091023002624N22
IRCT20091023002624N22已完成2 期

A comparison between the effect of tranexamic acid and placebo on the amount of hemorrhage in women following vaginal delivery and its adverse effects.

Iran University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
200

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
18 years 至 45 years(—)
性别
Female

入选标准

  • gestational age between 37-42 weeks
  • normal blood pressure (< 140/90 mmHg)
  • informed consent for the study

排除标准

  • history of coagulopathy
  • pre-eclampsia
  • placental abruption
  • hypersensitivity to tranexamic acid
  • Body Mass Index(BMI) of more than 30
  • history of cardiac, hepatic, renal and neurologic disorders

研究者

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