ISRCTN11204890已完成2 期
Efficacy of preoperative Tranexamic acid in reducing blood at Caesarean section; a randomized controlled trial at Irrua, Edo state.
Irrua Specialist Teaching Hospital0 个研究点目标入组 208 人开始时间: 2019年4月4日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 208
研究概览
简要总结
2021 Results article in https://drive.google.com/file/d/1DmGJskKwH1g2TF6N6w5BgFf_tem-ONpg/view?usp=sharing (added 28/12/2022)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. All pregnant women scheduled for a primary Caesarean section
- •2. Singleton pregnancy
排除标准
- •1. Multiple gestation
- •2. Any other additional risk of bleeding apart from the Caesarean section such as previous caesarean section, antepartum haemorrhage, polyhydramnios and bleeding disorders.
- •3. Liver or Renal pathologies
- •4. Patients who chose not to participate in the study.
- •5. Allergy to Tranexamic acid
- •6. Women unfit to give an informed consent e.g. the eclamptic, unconscious or those with mental impairment.
研究者
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