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临床试验/EUCTR2013-003547-39-NL
EUCTR2013-003547-39-NL进行中(未招募)不适用

Dexmedetomidine vs. clonidine in delirious intensive care patients: a randomised open-label trial

Isala Klinieken0 个研究点开始时间: 2013年9月17日最近更新:
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

  • - age > 18
  • - no response on treatment with haloperidol (max. dose till 3x5mg)
  • - positive score CAM-ICU
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

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

发起方
Isala Klinieken

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