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临床试验/NCT06085027
NCT06085027尚未招募不适用

Compare the Epifaith® Syringe With the Plastic Syringe for Identification of the Epidural Space in Parturients: A Prospective Randomized Control Study

Chang Gung Memorial Hospital0 个研究点目标入组 300 人开始时间: 2023年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
300
主要终点
Time consumed to identify the epidural space

研究概览

简要总结

The goal of this clinical trial is to compare the efficiency of identifying epidural space with either the Epifaith® syringe or the plastic syringe in parturients. The main questions it aims to answer are:

  • Whether it consume less time identifying epidural space with the Epifaith® syringe
  • Whether the usage of the Epifaith® syringe decrease the complication rate and failure of labor analgesia Participants will receive labor analgesia either with the Epifaith® syringe or the plastic syringe conducted by experienced resident doctors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • ASA II to III
  • Require labor analgesia
  • Has submitted inform consent

排除标准

  • ASA IV or above
  • Coagulopathy
  • Spinal deformity
  • Neurological, psychological, cardiopulmonary disorder
  • Active liver or kidney injury

结局指标

主要结局

Time consumed to identify the epidural space

时间窗: During the procedure

Starting on the moment which the syringe be attached to the needle

次要结局

未报告次要终点

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Sponsor

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