IRCT2012072910324N2已完成未知
The effect of intravenous tranexamic acid on blood loss after vaginal delivery: A Randomized Controlled Trial
Womens Reproductive Health Research center, Tabriz University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:
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 years 至 35 years（—）
- 性别
- Female
入选标准
- •-Women with singleton pregnancy between 38 to 42 weeks
- •- Cephalic presentation
- •- No history of cesarean section or uterine surgery
- •- No history of uterine myoma
- •- Normal blood pressure
- •- No history of postpartum haemorrhage
- •- No history of coagulation disorders
- •- No history of heart disease
- •- No history of renal disease
- •- No history of blood disorders and anemia
- •- No history of cerebrovascular disease
- •- Absence of diabetes and preeclampsia in pregnancy current
- •- Absence of polyhydramnious of macrosomia in the current pregnancy
- •- lack of long-term induction of labor in first stage
- •Exclusion criteria:
- •- Instrumental delivery
- •- Extensive vaginal and cervical lacerations
- •- Need for placenta curettag
- •- Continuous pressure in the fundus of the uterus before the fetus and placenta expulsion.
排除标准
- 未提供
研究者
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