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临床试验/PACTR201804002955302
PACTR201804002955302已完成未知

EFFECT OF INTRAVENOUS TRANEXAMIC ACID IN REDUCING BLOOD LOSS DURING CAESAREAN DELIVERY: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIA

niversity College Hospital0 个研究点目标入组 71 人开始时间: 2018年1月9日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
71

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 Year(s) 至 45 Year(s)(—)
性别
Female

入选标准

  • Pregnant women scheduled for primary elective or emergency caesarean delivery

排除标准

  • 1.Severe medical and surgical complications involving the heart, liver or kidney, and blood disorder.
  • 2.Allergy to tranexamic acid.
  • 3.Known risk factors for postpartum haemorrhage such as previous caesarean delivery, multiple pregnancy, placenta praevia, morbidly adherent placenta, previous myomectomy, co-existing uterine fibroid in pregnancy.
  • 4.History of thrombo-embolic disorder or risk factors for thromboembolic disorder such as Sickle Cell disease.
  • 5.Refusal to consent.

研究者

发起方
niversity College Hospital

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