ISRCTN68599804已完成未知
Safety and Effectiveness using DEXmedetomidine sedation versus propofol/alfentanil sedation during oesophagus interventions
Academic Medical Centre (AMC) (Netherlands)0 个研究点目标入组 64 人开始时间: 2013年4月16日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 64
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Eligible patients for participation in this clinical trial are those planned to undergo elective endoscopic oesophagus intervention. The patients must comply with the following criteria in order to be eligible to participate in this clinical study:
- •1. Male and female, age range = 18 years without upper age limit
- •2. ASA classification I ? III
- •3. Written informed consent
排除标准
- •1. Age range < 18 years
- •2. ASA classification IV and V
- •3. Allergic reaction to planned medication in the patients? medical history
- •4. Unregulated hypertension
- •5. Hypovolemia or hypotension (systolic blood pressure <80 or mean arterial pressure <50 mmHg)
- •6. Severe bradycardia (heart rate < 50/min) and / or related brady-dysrhythmias (e.g. advanced heart block)
- •7. Impaired ventricular function (left ventricular ejection fraction <30%)
- •8. Impaired renal function, GFR less than 15ml/min or undergoing hemodialysis
- •9. Impaired liver function
- •10. Substance abuse
研究者
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