EUCTR2005-003516-29-DE进行中（未招募）不适用
Prospective, randomized, double-blinded clinical trial on remifentanil for analgesia and sedation of ventilated neonates and infants - RAPIP-Pilotstudie
niversität zu Köln0 个研究点开始时间: 2006年10月20日最近更新:
适应症
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
- •Ventilated term newborns and infants < 60 days.
- •Expected time of artificial ventilation between 12 and 96 hours.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Various conditions of neuromuscular impairment e.g. severe peripartal asphyxia, cerebral infarct, congenital muscular diseases or metabolic defects showing distinct neuromuscular symptoms.
- •Drug abuse of the mother (exclusion criterion for newborns).
- •Known hypersensitivity to Ultiva®, Fentanyl-Janssen® or fentanyle equivalents.
- •Missing informed consent of the parents.
- •Participation in another clinical trial during or within the last 4 weeks before start of this trial.
研究者
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