EUCTR2009-013293-41-GB进行中（未招募）1 期
Randomised, double blind, phase IV study to compare the incidence of ECG changes during elective caesarean section under spinal anaesthesia when using phenylephrine or ephedrine infusion to maintain baseline systolic blood pressure - Ephedrine vs phenylephrine – ECG changes. V1
Joint UCLH/UCH Biomedical Research Unit0 个研究点目标入组 220 人开始时间: 2010年12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
- 220
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
- 性别
- Female
入选标准
- •Inclusion Criteria:
- •>37/40 weeks gestation
- •Singleton pregnancy
- •Elective caesarean section under spinal anaesthesia
- •In good general health (American Society of Anesthesiologists health status category 1 or 2)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Exclusion Criteria:
- •Circulatory disease (eg pre-existing hypertension)
- •Cardiac disease/medications (eg.angina, cardiomyopathy, B Blocker
- •medication)
- •Pregnancy related disease (pre-eclampsia)
- •. Diabetes that pre-exists the pregnancy
- •. Renal disease
- •. Hyperthyroidism
- •. Closed angle glaucoma
- •In active labour
- •Emergency caesarean section
- •Fetal abnormalities
- •Contraindications to spinal anaesthesia
- •Height >6 feet/180cm / Height <5 feet/150cm
- •BMI <19 or >35
- •Patient refusal to participate
研究者
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