CTRI/2024/04/066348尚未招募2/3 期
Effect of prophylactic tranexamic acid in reducing postpartum blood loss in vaginal deliveries at tertiary care centre; placebo controlled randomized clinical trial
DR SN MEDICAL COLLEGE1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年5月1日最近更新:
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- To quantify the mean 2hour postpartum blood loss
研究概览
简要总结
Intravenous infusion of 1 gm Tranexamic acid in 10 ml diluent over 10 minutes will be given to the patients at the time of delivery.
Aim of the study is to minimize the mortality and morbidity due to postpartum blood loss.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 19.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •prmigravida or secondary gravida 37 to 42 weeks of gestation admitted in active labour normotensive cephalic presentation.
排除标准
- •All other patients not fulfilling the inclusion criteria.
结局指标
主要结局
To quantify the mean 2hour postpartum blood loss
时间窗: from delivery to 2 hour postpartum
次要结局
- To see if any other intervention needed after delivery & to compare the need of blood transfusion & to see the potential adverse effects of tranexamic acid.
研究者
Dr Seema
DR SN MEDICAL COLLEGE
研究点 (1)
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