EUCTR2013-005617-13-BE进行中（未招募）不适用
Determination of the equivalent dose of phenylephrine and Akrinor in the prevention of post-spinal hypotension during Cesarean section.
niversity Hospitals Leuven0 个研究点开始时间: 2014年2月6日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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
- •- Elective Cesarean section
- •- Singleton pregnancies
- •- >36 weeks
- •- >18 years
- •- ASA 1-2
- •- 50-120 kg
- •- 150-180 cm
- •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 60
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Pregnancy induced hypertension
- •- Diabetes mellitus
- •- Cardiovascular and cerebrovascular problems
- •- Prenatally diagnosed foetal abnormalities
- •- Contra-indications for spinal anesthesia
- •- Active labour
研究者
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Evaluation of equivalent effective dose of ephedrine and phenylephrine in prevention of hypotension after spinal anaesthesia for caesarean sectioISRCTN62049497Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)