IRCT2013100914961N1已完成2 期
Comparison of efficacy of combination diclofenac suppository and tranxamic acid with diclofenac suppository and tranxamic acid alone on pain and bleeding in patients undergoing spinal anesthesia for cesarean tostoperative bleeding in patients undergoing spinal anesthesia for cesarean
The school of Medicine of Qazvin0 个研究点目标入组 210 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 210
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 years 至 40 years（—）
- 性别
- Female
入选标准
- •pregnant women aged 18 to 40 years ; selection for cesarean section; full satisfaction of the spinal anesthesia;have no underlying disease; don’t have any prohibition for spinal anesthesia and allergy to anesthetics and the other drugs;not using Hypnotics and anti-anxiety drugs Exclusion criteria: presence of underlying disease;prohibition to spinal anesthesia and allergy to anesthetics and the other drugs; using hypnotics and anti-anxiety drugs; patients with hemoglobin less than 10;patients with detached placenta, placenta Acreta, placenta previa;multiple;history of thromboembolic disease ;any coagulopathy; patients with a BMI over 35 ; kidney trouble;polyhydroamnious and oligo hydroamnious
排除标准
- 未提供
研究者
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