PACTR202306670143734尚未招募Unknown
The effect of two varying doses of intravenous tranexamic acid on blood loss after vaginal delivery at term in University of Benin Teaching Hospital: a double-blinded randomized placebo-controlled trial
未提供0 个研究点目标入组 135 人开始时间: 2023年6月26日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 入组人数
- 135
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •All women with gestation age between 37 completed weeks to 41weeks and 6days and Parity 0-4 admitted in labour (spontaneous labour or induction of labour)
- •Gave consent for the study
- •Had vaginal delivery
排除标准
- •Any woman with gestation age between 37 completed weeks to 41weeks and 6days admitted in labour (spontaneous labour or induction of labour) who did not give consent for the study
- •Any woman who has history of thrombosis or epilepsy, history of medical/surgical conditions involving the heart, liver, kidney and brain, have known allergy to tranexamic acid, and bleeding disorders and abnormalities before pregnancy.
- •Eventually delivered by Caesarean section after meeting inclusion criteria
研究者
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