CTRI/2024/04/066132尚未招募3 期
A randomised controlled trial to compare the efficacy of carbetocin vs oxytocin in preventing postpartum hemorrhage in women undergoing vaginal delivery - Nil
Esther Issac0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
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
入选标准
- •Singleton pregnancies
- •Undergoing vaginal delivery
排除标准
- •Patients with one or more of following were excluded:
- •underlying medical disease, including severe pre-eclampsia, eclampsia,bleeding disorders, thrombocytopenia, cardiovascular diseases, liver and renal diseases.
- •(2) history of oxytocin or carbetocin allergy
- •(3) obstetric complications, such as placental abruption and abnormal placentation.
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