NL-OMON33849已完成3 期
A PROSPECTIVE, MULTI-CENTRE, RANDOMISED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS DEXMEDETOMIDINE WITH MIDAZOLAM FOR CONTINUOUS SEDATION OF VENTILATED PATIENTS IN INTENSIVE CARE UNIT - MiDex
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 175
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
- 年龄范围
- 18 至 99（—）
入选标准
- •Patients >=18 years, Clinical need for sedation or intubated, RASS = 0 to -3 (light to moderate sedation), patient should have an expected requirement for sedation >= 24 hours, Written informed consent
- •protocol p. 23-24
排除标准
- •Acute severe intracranial or spinal neurological disorder, Uncompensated acute circulatory failure, Severe bradycardia, AV-conduction block II-III, Severe hepatic impairment, Need for muscle relaxation, Loss of hearing or vision, Burn injuries and other injuries requiring regular anaesthesia or surgery, Use of centrally acting a2-agonists or antagonists within 24 hours prior to randomisation
研究者
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