NL-OMON38662已完成4 期
Dexmedetomidine vs. clonidine in delirious intensive care patients: a randomised open-label trial - The effect of dexmedetomidine and clonidine on delirium
Isala Klinieken0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 24
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
- •- age > 18
- •- no response on treatment with haloperidol (max. dose till 3x5mg)
- •- positive score CAM-ICU
排除标准
- •- history of epilepsy, Parkinson's disease, hypokinetic rigid syndrome, or Lewy body dementia
- •- treatment with antipsychotic drugs
- •- pregnancy or breastfeeding
- •- CVA < 6months
- •- hypotension (< 90mmHg)
- •- bradycardia (<50/min)
- •- MAP < 60mmHg
- •- comatose patients (RASS -4 or -5)
- •- recent myocardial infarction of severe coronal insufficiency
- •- 2nd of 3rd degree AV-block or sicksinussyndrome
- •- known allergic reaction on clonidine of dexmedetomidine
研究者
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