EUCTR2016-003010-26-BE进行中（未招募）1 期
Hyperbaric Bupivacaine Versus Hyperbaric Prilocaine 2% for Cesarean Section Under Spinal Anesthesia: a Randomised and Controlled Clinical Trial
Centre Hospitalier Universitaire Saint Pierre , ULB0 个研究点目标入组 100 人开始时间: 2017年12月6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
- 性别
- Female
入选标准
- •American Society of Anesthesiologists physical status (ASA) < III
- •Age 18-40 year
- •Body Weight <110 kg
- •Height between 160 and 175 cm
- •Gestational age>37 SA
- •Elective cesarean delivery
- •Singleton pregnancy
- •Non complicated pregnancy
- •Signed informed consent obtained prior to any study specific assessments and procedures
- •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 100
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Twin pregnancy
- •History of 2 cesarean section or more
- •Diabetes and gestational diabetes
- •Placenta praevia
- •Congenital foetale abnormality
- •Intrauterine growth retardation
- •Patient in labour
- •Membrane rupture
- •Known allergy to local anaesthetics
- •Standard contraindications to neuraxial block.
- •Disagreement of the patient
- •Neurological impairment
- •Gestational low blood pressure
- •Pre eclampsia and eclampsia
研究者
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