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A Comparison of Dexmedetomidine and Haloperidol in Patients With Intensive Care Unit (ICU)-Associated Agitation and Delirium (Dex)

Primary Purpose

Delirium, Agitation, Ventilator Weaning

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
dexmedetomidine
haloperidol
Sponsored by
Austin Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Delirium focused on measuring dexmedetomidine, haloperidol

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    1

    2

    Arm Description

    Outcomes

    Primary Outcome Measures

    Time from the commencement of treatment to extubation
    the tiem taken to extubate the patient

    Secondary Outcome Measures

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

    Full Information

    First Posted
    July 23, 2007
    Last Updated
    January 22, 2013
    Sponsor
    Austin Health
    Collaborators
    The Alfred
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00505804
    Brief Title
    A Comparison of Dexmedetomidine and Haloperidol in Patients With Intensive Care Unit (ICU)-Associated Agitation and Delirium
    Acronym
    Dex
    Official Title
    A Randomised Open Label Pilot Study of the Efficacy of Dexmedetomidine and Haloperidol in Ventilated Patients With ICU-associated Agitation and Delirium
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2013
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2005 (undefined)
    Primary Completion Date
    November 2008 (Actual)
    Study Completion Date
    November 2008 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Austin Health
    Collaborators
    The Alfred

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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.
    Detailed Description
    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.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Delirium, Agitation, Ventilator Weaning, Respiration, Artificial, Intensive Care
    Keywords
    dexmedetomidine, haloperidol

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    20 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Title
    2
    Arm Type
    Active Comparator
    Intervention Type
    Drug
    Intervention Name(s)
    dexmedetomidine
    Intervention Description
    Dexmedetomidine IV infusion of 0.0 to 0.7 mg/kg/min for as long a deemed necessary by the treating clinician.
    Intervention Type
    Drug
    Intervention Name(s)
    haloperidol
    Intervention Description
    Haloperidol IV loading dose of 2.5mg, followed by a continuous infusion of 0.0 to 2mg/hr for as long as deemed necessary by the treating clinician
    Primary Outcome Measure Information:
    Title
    Time from the commencement of treatment to extubation
    Description
    the tiem taken to extubate the patient
    Time Frame
    days
    Secondary Outcome Measure Information:
    Title
    Time taken to achieve a satisfactory sedation score (score 3 or 4 on the Riker scale)
    Description
    time to sedation score
    Time Frame
    hours
    Title
    The need for supplemental sedative and analgesic medication (morphine, midazolam or propofol, as clinically indicated)
    Time Frame
    During delivery of trial medication
    Title
    Average Riker score for agitation
    Time Frame
    During delivery of trial medication
    Title
    Average RASS score for agitation
    Time Frame
    During delivery of trial medication
    Title
    Need for re-intubation
    Time Frame
    During the same ICU admission
    Title
    Average Bergeron ICDSC score for delirium
    Time Frame
    During delivery of trial medication
    Title
    Duration of ICU stay
    Time Frame
    days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 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. Exclusion Criteria: 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
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rinaldo Bellomo, MD FJFICM
    Organizational Affiliation
    Austin Health, University of Melbourne
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Michael C Reade, MBBS FJFICM
    Organizational Affiliation
    Austin Health, University of Melbourne
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    19454032
    Citation
    Reade MC, O'Sullivan K, Bates S, Goldsmith D, Ainslie WR, Bellomo R. Dexmedetomidine vs. haloperidol in delirious, agitated, intubated patients: a randomised open-label trial. Crit Care. 2009;13(3):R75. doi: 10.1186/cc7890. Epub 2009 May 19.
    Results Reference
    derived

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    A Comparison of Dexmedetomidine and Haloperidol in Patients With Intensive Care Unit (ICU)-Associated Agitation and Delirium

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