跳至主要内容
临床试验/KCT0000715
KCT0000715已完成未知

Haemodynamic effects of carbetocin given as i.v. bolus or infusion on women undergoing caesarean delivery.

Dongguk University Ilsan Hospital0 个研究点目标入组 34 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
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
o Limit 至 o Limit(—)
性别
Female

入选标准

  • Healthy term parturients (37-41 weeks) with American Society of Anesthesiology Physical Status I and II, who were scheduled to undergo elective cesarean delivery under spinal anesthesia and to receive carbetocin.

排除标准

  • Women with preeclampsia, placenta previa, diabetes mellitus or hypertension which conditions could lead to cardiovascular instability

研究者

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