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临床试验/TCTR20221113003
TCTR20221113003招募中4 期

Comparison of oxytocin low-rate infusion versus oxytocin bolus for initiating uterine contraction during cesarean delivery: A randomized, controlled, non-inferiority trial

Khon Kaen University0 个研究点目标入组 160 人开始时间: 2022年11月13日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
160

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

  • Pregnancy aged 18-40 years old, GA 37-42 weeks, ASA ll, singleton, scheduled undergoing elective Cesarean delivery under spinal anesthesia

排除标准

  • Previous uterine surgery other than cesarean section, high risk of uterine atony (macrosomia, chorioamnionitis, polyhydramnios, uterine mass), high risk of postpartum hemorrhage (placenta previa or other placenta disorders, history of postpartum hemorrhage, coagulopathy, thrombocytopenia, pre-eclampsia)

研究者

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