EUCTR2013-000485-11-BE进行中（未招募）1 期
Xenon as an adjuvant to propofol anaesthesia in patients undergoing off-pump coronary artery bypass graft surgery: a randomized controlled trial
niversity Hospitals of the KU Leuven0 个研究点目标入组 50 人开始时间: 2013年3月20日最近更新:
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
- 50
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
- •Patients with coronary artery disease scheduled for elective OPCAB-surgery
- •Patients willing and able to complete the requirements of this study
- •Ejection Fraction > 30%
- •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 25
排除标准
- •Lack of informed consent
- •Age < 18 years
- •COPD GOLD > II
- •Renal dysfunction defined as serum-creatinine > 1.5 mg/dl
- •Acute coronary syndrome during the last 24 hours; haemodynamic instability, requirement of inotropic support
- •Single vessel grafting
- •Disabling neuropsychiatric disorders (severe dementia, Alzheimer’s disease, schizophrenia, depression), low preoperative cognitive state (MMSE at baseline <25), history of stroke with residuals, increased intracranial pressure
- •Hypersensitivity to the study medication
- •Presumed uncooperativeness or legal incapacity
研究者
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