EUCTR2015-000537-69-BE进行中(未招募)1 期
Real time monitoring of blood propofol concentration
niversitair Ziekenhuis Brussel0 个研究点目标入组 30 人开始时间: 2015年8月24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
- 30
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
- All
入选标准
- •- >18-70 years
- •- ASA I, II
- •- Weight not exceeding 50 % under or above normal ideal body weight
- •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 25
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 5
排除标准
- •- Pregnancy
- •- ASA III and ASA IV
研究者
相似试验
Unknown
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REAL-TIME BEDSIDE MONITORING OF BLOOD PROPOFOL CONCENTRATIONS:Blood propofol concentrationsIntrancranial neurosurgical interventionear surgeryNociceptionInfluence of opioid supplementationNL-OMON25330niversitair Ziekenhuis BrusselLaarbeeklaan 101 1090 Jette24
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Significant decreases in blood propofol concentrations during adrenalectomy for phaeochromocytomapheochromocytomaJPRN-UMIN000008733Department of Anesthesiology Niigata University Graduate School of Medical and Dental Sciences20
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Target controlled infusion for propofol anesthesia during Transjugular Intrahepatic Porto Systemic Shunt procedureAnaesthesiaPACTR202310626983365natioanl liver institute78
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不适用
Blood Propofol Measurement During Anaesthesia Using Propofol Target Controlled InfusionGeneral AnaesthesiaPropofolTarget Controlled InfusionPharmacokineticsNCT01549639University Hospital Birmingham NHS Foundation Trust50
