跳至主要内容
临床试验/KCT0007756
KCT0007756已完成未知

Comparison of programmed intermittent epidural bolus injection vs. continuous epidural infusion for post cesarean delivery analgesia: A randomized controlled trial

Samsung Medical Center0 个研究点目标入组 74 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
74

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
19(Year) 至 45(Year)(—)
性别
Female

入选标准

  • age from 19 to 45 years
  • - 37 weeks or more of gestation
  • - American Society of Anesthesiologists physical status (ASA PS): II, III

排除标准

  • - American Society of Anesthesiologists physical status (ASA PS): IV or higher
  • - Age under the age of 19 or over 45 years
  • - twin pregnancy
  • - fetal malformations during prenatal screening.
  • - More than 3 deliveries
  • - body mass index (BMI) >40 kg/m2
  • - Patients who did not understand this study protocol or who declined to participate in the study
  • - Serious psychiatric disorders that may affect patient evaluation

研究者

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