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:
相关药物0.1% Bupivacaine
概览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- eeds Teaching Hospitals Trust
- 入组人数
- 100
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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