PACTR201706002304422已完成未知
Efficacy of tranexamic acid at reducing blood loss during elective caesarean section in Abakaliki: a randomized double blind placebo controlled trial
federal teaching hospital abakaliki0 个研究点目标入组 120 人开始时间: 2017年5月20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
- 120
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
- •1. Parturients with singleton pregnancy at 37-42 weeks¿ gestational age
- •2. Patient on admission for elective caesarean section
- •3. patients without contraindication to tranexamic acid
- •4. patient who have signed the informed consent
排除标准
- •1. Women who have known allergy to tranexamic acid
- •2. Women with prior history of thromboembolism
- •3. Women with bleeding disorders
- •4. Patients with renal disease
- •5. Patients with liver pathology
- •6. Patients with chronic hypertension
- •7. Patients with preeclampsia/eclampsia
- •8. Women with antepartum haemorrhage
- •9. Patients with varicose veins at increased risk of deep vein thrombosis
- •10. Patients who do not consent to the study.
研究者
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