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临床试验/CTRI/2023/05/053088
CTRI/2023/05/053088招募中4 期

Minimum effective dose of prophylactic oxytocin infusion during cesarean delivery: Comparison between patients with preterm versus term pregnancy - NI

niversity College of Medical Sciences and GTB Hospital0 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
4 期
状态
招募中
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

  • Posted for cesarean delivery under spinal block; either into the term or preterm cohort (defined as gestational age of completed 37 weeks (i.e., =259 days) or <37 weeks respectively.

排除标准

  • Laboring with preoperative oxytocin use, or magnesium sulfate therapy, coagulopathy, history of previous uterine atony or postpartum hemorrhage or bleeding disorder or heart disease.

研究者

发起方
niversity College of Medical Sciences and GTB Hospital

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