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Efficacy of Ketamine in Children With Severe Brain Injury for Brain Cell Protection

Primary Purpose

Traumatic Brain Injury

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
saline
Ketamine
Sponsored by
University of Arkansas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury focused on measuring traumatic brain injury

Eligibility Criteria

1 Month - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • are 1 month to 16 years of age; AND
  • are admitted to the PICU following severe TBI (any GCS 3-8 inclusive) within 8 hours after the injury; AND
  • are intubated and ventilated for the management of TBI; AND
  • are anticipated to have an indwelling arterial or venous catheter for blood sampling during the first three days of study enrollment; AND
  • have an intra-cranial pressure (ICP) monitoring device for management of TBI.

Exclusion Criteria:

  • are less than 4 kilograms in weight upon admission
  • are less than 1 month of age;
  • are greater than 16 years of age;
  • have a clinical diagnosis of non-accidental TBI;
  • have suffered immersion injury or prolonged hypoxic injury (lasting greater than 10 minutes);
  • have a known allergy to ketamine;
  • have a planned removal of endotracheal tube or the removal of central venous catheter AND arterial catheter within 72 hours of study enrollment;
  • have a current history of neuromuscular disease;
  • have a current history of hepatic failure;
  • have a current history of glaucoma
  • require chronic treatment with anti-epileptic drugs (AEDs) or devices;
  • more than 8 hours have elapsed from the time of injury to PICU admission;
  • have documentation of a positive pregnancy test at the time of enrollment;
  • if there is a lack of commitment to aggressive intensive care therapies (the subject is either on a DNR status due to pre-existing medical condition, or the family decides to withdraw support prior to participation in the study due to other multiple severe injuries and organ failures resulting from the trauma).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    1

    2

    Arm Description

    Placebo Group receiving Saline Infusion.

    Case Group receiving Ketamine infusion.

    Outcomes

    Primary Outcome Measures

    To compare clinical, radiological, and neurodevelopmental outcomes between children who receive ketamine vs placebo infusions following traumatic brain injury.

    Secondary Outcome Measures

    To compare the expression of biomarkers of CNS injury between cases and controls.

    Full Information

    First Posted
    November 9, 2007
    Last Updated
    October 31, 2013
    Sponsor
    University of Arkansas
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00556387
    Brief Title
    Efficacy of Ketamine in Children With Severe Brain Injury for Brain Cell Protection
    Official Title
    Possible Neuroprotective Effects of Ketamine in Children With Severe Traumatic Brain Injury
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2013
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    This study has been withdraw from the IRB. The PI has transferred to another university. The IND was transferred.
    Study Start Date
    December 2008 (undefined)
    Primary Completion Date
    December 2012 (Anticipated)
    Study Completion Date
    December 2012 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University of Arkansas

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to determine the possible effects of an anesthetic agent called Ketamine on the injured brain in children. The researchers think that it will effect the outcomes of children with these injuries.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Traumatic Brain Injury
    Keywords
    traumatic brain injury

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo Group receiving Saline Infusion.
    Arm Title
    2
    Arm Type
    Experimental
    Arm Description
    Case Group receiving Ketamine infusion.
    Intervention Type
    Drug
    Intervention Name(s)
    saline
    Intervention Description
    1 mg/kg IV bolus slowly over 1-2 minutes followed by 0.5 mg/kg IV continuous infusion over 48 hours or until discontinuation of ICP monitor (whichever occurs first)
    Intervention Type
    Drug
    Intervention Name(s)
    Ketamine
    Intervention Description
    1 mg/kg IV bolus slowly over 1-2 minutes, followed by 0.5 mg/kg IV continuous infusion for 48 hours or until discontinuation of ICP monitor (whichever occurs first)
    Primary Outcome Measure Information:
    Title
    To compare clinical, radiological, and neurodevelopmental outcomes between children who receive ketamine vs placebo infusions following traumatic brain injury.
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    To compare the expression of biomarkers of CNS injury between cases and controls.
    Time Frame
    96 hours

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Month
    Maximum Age & Unit of Time
    16 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: are 1 month to 16 years of age; AND are admitted to the PICU following severe TBI (any GCS 3-8 inclusive) within 8 hours after the injury; AND are intubated and ventilated for the management of TBI; AND are anticipated to have an indwelling arterial or venous catheter for blood sampling during the first three days of study enrollment; AND have an intra-cranial pressure (ICP) monitoring device for management of TBI. Exclusion Criteria: are less than 4 kilograms in weight upon admission are less than 1 month of age; are greater than 16 years of age; have a clinical diagnosis of non-accidental TBI; have suffered immersion injury or prolonged hypoxic injury (lasting greater than 10 minutes); have a known allergy to ketamine; have a planned removal of endotracheal tube or the removal of central venous catheter AND arterial catheter within 72 hours of study enrollment; have a current history of neuromuscular disease; have a current history of hepatic failure; have a current history of glaucoma require chronic treatment with anti-epileptic drugs (AEDs) or devices; more than 8 hours have elapsed from the time of injury to PICU admission; have documentation of a positive pregnancy test at the time of enrollment; if there is a lack of commitment to aggressive intensive care therapies (the subject is either on a DNR status due to pre-existing medical condition, or the family decides to withdraw support prior to participation in the study due to other multiple severe injuries and organ failures resulting from the trauma).
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Muayyad Tailounie, MD
    Organizational Affiliation
    Arkansas Children's Hospital Research Institute
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Efficacy of Ketamine in Children With Severe Brain Injury for Brain Cell Protection

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