ACTRN12609000041257尚未招募4 期
Comparison of the EpiSure Autodetect syringe with the conventional loss-of-resistance syringe among parturients in labour: a randomised controlled trial of analgesic proficiency
King Edward Memorial Hospital for Women0 个研究点目标入组 1,000 人开始时间: 2009年1月19日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Epidural analgesia for labour
- •American Society of Anesthesiologists (ASA) Classification I to III patients
排除标准
- •Combined spinal and epidural
- •Fetal abnormality
- •Contraindication to epidural analgesia
- •Spinal abnormaility
- •Body mass index (BMI) above 44
研究者
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