TCTR20170702001Enrolling By Invitation2 期
Double-blind randomized comparison of carbetocin versus oxytocin for decrease blood loss from cesarean section in low-risk uterine atony
faculty of medicine Vajira hospital0 个研究点目标入组 122 人开始时间: 2017年7月2日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 122
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 50 Years（—）
- 性别
- Female
入选标准
- •1. At least 18 years old
- •2. singleton term uncomplicated pregnancy (37-42 weeks)
- •3. indication for cesarean section
- •4. regional anesthesia (carbetocin is licensed for use with regional anesthesia only)
排除标准
- •1.contraindications to use uterotonic drugs (heart disease, high blood pressure, allergic medicine)
- •2.severe anemia (Hb ≤ 8 gm / dl)
- •3.Disease or used drug that results abnormal blood bleeding
- •4.fetal distress
- •5.High risk for PPH due to uterine atony
- •â€¢prolong latent phase of labor
- •â€¢history of PPH
- •â€¢multiparity (childbirths >4 )
- •â€¢massive blood loss before labor
- •â€¢placenta previa
- •â€¢placental abruption
- •â€¢ placenta adherence
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