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临床试验/NCT00505804
NCT00505804已完成2 期

A Randomised Open Label Pilot Study of the Efficacy of Dexmedetomidine and Haloperidol in Ventilated Patients With ICU-associated Agitation and Delirium

Austin Health0 个研究点目标入组 20 人开始时间: 2005年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Austin Health
入组人数
20
主要终点
Time from the commencement of treatment to extubation

研究概览

简要总结

The purpose of the study is to determine whether dexmedetomidine is a more effective medication than haloperidol in the treatment of agitation and delirium in patients receiving mechanical ventilation in an intensive care unit. Haloperidol is a medication conventionally used for this purpose.

The investigators will study only patients who have recovered from their illness to the point that, were it not for agitation and delirium, they would no longer require mechanical ventilation.

The investigators hypothesize that patients receiving dexmedetomidine will be able to discontinue mechanical ventilation earlier than those receiving haloperidol.

详细描述

Up to 80% of patients undergoing intensive care have delirium. Early in the ICU stay, delirium and agitation are usually prevented using analgesic and sedative drugs which essentially render the patient unconscious. This is appropriate in the context of aggressive treatment of pathophysiological instability, which often requires multiple painful procedures. However, after the underlying pathophysiological problem has resolved, patients sometimes remain delirious and agitated. This often requires ongoing heavy sedation, which in turn necessitates continued mechanical ventilation, and can worsen the (temporarily masked) delirium. Prolonged mechanical ventilation increases the risk of ventilator associated pneumonia and other life threatening complications.

The drug most commonly used to treat delirium is haloperidol, which reduces hallucinations and unstructured thought patterns, but also reduces the interaction with the environment. Haloperidol has significant side effects, including extrapyramidal reactions (in 1-10% of patients), neuroleptic malignant syndrome (in which it is the cause in 50% of cases), and prolonged QT syndrome (which can precipitate fatal arrhythmias).

An ideal sedative agent in this context would have fewer side effects, relieve agitation without causing excessive sedation, and be easily titrated. An analgesic action might allow less opioid use, also lessening delirium. Early studies in other contexts suggest dexmedetomidine has all these properties.

The investigators hypothesise that patients with ICU-associated delirium after the resolution of their underlying pathological process who receive dexmedetomidine will be able to be extubated earlier than those who receive haloperidol.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients will be eligible for the study if, in the opinion of the treating clinician, they continue to require mechanical ventilation only because their degree of agitation requires such a high dose of sedative medication (midazolam or propofol, the only commonly used specific sedatives in our unit) that extubation is not possible.

排除标准

  • Patients who could not be extubated even if delirium or agitation were corrected. This will include:
  • Patients receiving high dose opioid analgesia (>20 m/morphine/day)
  • Patients shortly to return to the operating theatre
  • Patients undergoing repeated invasive procedures, in whom it is desirable to maintain deep sedation.
  • Patients likely to require ongoing airway protection or control, or ventilatory support (for example, spinal patients with an inadequate vital capacity)
  • Known allergy to haloperidol or alpha2 agonists

研究组 & 干预措施

1

Experimental

干预措施: dexmedetomidine (Drug)

2

Active Comparator

干预措施: haloperidol (Drug)

结局指标

主要结局

Time from the commencement of treatment to extubation

时间窗: days

the tiem taken to extubate the patient

次要结局

  • Average RASS score for agitation(During delivery of trial medication)
  • Average Bergeron ICDSC score for delirium(During delivery of trial medication)
  • Duration of ICU stay(days)
  • Average Riker score for agitation(During delivery of trial medication)
  • Need for re-intubation(During the same ICU admission)
  • Time taken to achieve a satisfactory sedation score (score 3 or 4 on the Riker scale)(hours)
  • The need for supplemental sedative and analgesic medication (morphine, midazolam or propofol, as clinically indicated)(During delivery of trial medication)

研究者

发起方
Austin Health
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Rinaldo Bellomo

Prof

Austin Health

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