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
- 是
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
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