EUCTR2010-020020-21-GB进行中（未招募）1 期
Comparison of the ED95 dose of 0.075% and 0.1% bupivacaine for labour analgesia in primigravida - MED and Epidural Bupivacaine
eeds Teaching Hospitals Trust0 个研究点目标入组 100 人开始时间: 2011年4月15日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •ASA 1-3 patients
- •Age > 18 years
- •Primigravida (1st pregnancy) patients requesting epidural analgesia in early labour (= 5 cm cervical dilatation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Primigravida (1st pregnancy) patients requesting epidural analgesia in late labour (> 5 cm cervical dilatation)
- •Multigravida patients ( = 2nd pregnancy)
- •Age < 18 years
- •Allergy to Bupivacaine
- •Unable to give written informed consent
- •Abnormal blood coagulation profile
- •Patients taking any medication that are indicated in the SPC as not recommended
研究者
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