NL-OMON31109已完成3 期
A PROSPECTIVE, MULTI-CENTRE, RANDOMISED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS DEXMEDETOMIDINE WITH PROPOFOL FOR CONTINUOUS SEDATION OF VENTILATED PATIENTS IN INTENSIVE CARE UNIT - ProDex
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 100
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
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, Use of centrally acting a2-agonists or antagonists
研究者
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A PROSPECTIVE, MULTI-CENTRE, RANDOMISED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS DEXMEDETOMIDINE WITH PROPOFOL FOR CONTINUOUS SEDATION OF VENTILATED PATIENTS IN INTENSIVE CARE UNIT - ProdexPatients requiring mechanical ventilation and sedation in ICU.MedDRA version: 8.0Level: LLTClassification code 10039897EUCTR2006-006030-17-NLOrion Corporation Orion Pharma500
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A PROSPECTIVE, MULTI-CENTRE, RANDOMISED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS DEXMEDETOMIDINE WITH MIDAZOLAM FOR CONTINUOUS SEDATION OF VENTILATED PATIENTS IN INTENSIVE CARE UNIT - MidexPatients requiring mechanical ventilation and sedation in ICU.MedDRA version: 8.0Level: LLTClassification code 10039897EUCTR2006-006031-50-FIOrion Corporation Orion Pharma500