EUCTR2012-002316-12-BE进行中（未招募）不适用
The safety and feasibility of administering xenon to patients undergoing off-pump coronary artery bypass graft surgery: a pilot studyXOPCAB – Xenon in Off-Pump Coronary Artery Bypass Grafting - XOPCAB – Xenon in Off-Pump Coronary Artery Bypass Grafting
niversity Hospitals of the KU Leuven0 个研究点开始时间: 2012年7月23日最近更新:
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
- 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 20
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •- Lack of informed consent
- •- Age < 18 years
- •- Pregnancy
- •- 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), 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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