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The Role of Ketamine as an Adjuvant Therapy for Children With Acute Status Asthmaticus

Primary Purpose

Status Asthmaticus

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Ketamine
Sponsored by
Augusta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Status Asthmaticus focused on measuring ketamine, pediatric status asthmaticus

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pediatric patients (≥2 years and ≤ 18 years old)

Patients presenting in status asthmaticus:

  • Patients with a CAS of greater than or equal to 10 on presentation that have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival

OR

  • Patients with a CAS of greater than or equal to 10 that have not received treatment prior to arrival and after 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2

OR

  • Patients with a CAS above 6 but less than 10 as measured 1 hour after initiation of standard treatment per AU's moderate asthma pathway

Exclusion Criteria:

  • Pregnancy
  • Congestive Heart Failure or prior diagnosis of cardiovascular disease (congenital or acquired)
  • Chronic lung disease outside of a previous diagnosis of Asthma
  • Seizure disorder
  • Liver disease
  • History of hypertension greater than 95% for age
  • Obstructive Sleep Apnea with AHI greater than 5
  • History of allergic or serious reaction to Ketamine
  • Significant history of psychiatric illness defined as any patient with a diagnosis of psychiatric illness meeting the Diagnostic and Statistical Manual of Mental Disorders V criteria (severe Autism)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Ketamine Treatment

    Arm Description

    Everyone enrolled in study presenting in status asthmaticus to pediatric emergency department at Augusta University will receive a ketamine treatment, who include: Patients with a Clinical Asthma SCore (CAS) of greater than or equal to 10 on presentation and have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival OR Patients with a CAS of ≥ greater than or equal to 10 that have not received treatment prior to arrival and after receiving 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2 OR Patients with a CAS above > 6 but less than < 10 when as measured 1 hour after initiation of standard treatment per Augusta University's moderate asthma pathway

    Outcomes

    Primary Outcome Measures

    Efficacy of ketamine in status asthmaticus by assessing change in clinical asthma score (CAS)
    CAS will be documented on admission, prior to intervention, 30 minutes and 60 minutes after administration of ketamine. The CAS is a scoring system to assess the severity of asthma used by Augusta University and is based on physiological measurements and clinical appearance.

    Secondary Outcome Measures

    Full Information

    First Posted
    November 1, 2017
    Last Updated
    July 15, 2019
    Sponsor
    Augusta University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03338205
    Brief Title
    The Role of Ketamine as an Adjuvant Therapy for Children With Acute Status Asthmaticus
    Official Title
    The Role of Ketamine as an Adjuvant Therapy for Children With Acute Status Asthmaticus in Pediatric Emergency Medicine Patients: A Pilot Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2020 (Anticipated)
    Primary Completion Date
    December 2021 (Anticipated)
    Study Completion Date
    January 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Augusta University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this investigation is to perform a pilot study assessing the safety and utility of intravenous ketamine as an adjuvant therapy in the emergency department setting for pediatric patients in acute status asthmaticus who have failed standard emergency therapy.
    Detailed Description
    This is a pilot study of a cohort of 20 subjects to assess the feasibility, safety and efficacy of ketamine in status asthmaticus. The study will take place at the Augusta University's pediatric emergency department 24 hours a day. The attending physician who is clinically treating the patient will identify the patient as a potential study candidate (see inclusion criteria). Study team members will then be notified and obtain informed consent for potential participants who meet the inclusion/exclusion criteria. Once a patient in the Augusta University Children's Hospital of Georgia Pediatric Emergency Department is deemed a potential study subject, informed consent will be obtained by the research study team members. The patient and their parents will be provided with all the required information about the study including potential risks and benefits associated with participation. The information will be presented in a private setting in a language the patient understands. The patient and/or their parent/guardian will have opportunities to ask questions and will be given enough time to consider participation before providing consent. A document will be given to obtain assent/consent that reiterates all the information about the study (including reason for the study, risks, benefits, etc.) Study team members that will be actively involved in the study will be either pediatric emergency medicine faculty or pediatric emergency medicine fellows that are on staff. Patients that meet the inclusion and exclusion criteria will have ketamine 1 mg/kg IV bolus administered once informed consent has been obtained.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Status Asthmaticus
    Keywords
    ketamine, pediatric status asthmaticus

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Single Group Assignment
    Model Description
    Pilot study
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    20 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Ketamine Treatment
    Arm Type
    Experimental
    Arm Description
    Everyone enrolled in study presenting in status asthmaticus to pediatric emergency department at Augusta University will receive a ketamine treatment, who include: Patients with a Clinical Asthma SCore (CAS) of greater than or equal to 10 on presentation and have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival OR Patients with a CAS of ≥ greater than or equal to 10 that have not received treatment prior to arrival and after receiving 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2 OR Patients with a CAS above > 6 but less than < 10 when as measured 1 hour after initiation of standard treatment per Augusta University's moderate asthma pathway
    Intervention Type
    Drug
    Intervention Name(s)
    Ketamine
    Intervention Description
    1 mg/kg ketamine bolus IV
    Primary Outcome Measure Information:
    Title
    Efficacy of ketamine in status asthmaticus by assessing change in clinical asthma score (CAS)
    Description
    CAS will be documented on admission, prior to intervention, 30 minutes and 60 minutes after administration of ketamine. The CAS is a scoring system to assess the severity of asthma used by Augusta University and is based on physiological measurements and clinical appearance.
    Time Frame
    prior to intervention, 30 minutes and 60 minutes after administration of ketamine

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    2 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Pediatric patients (≥2 years and ≤ 18 years old) Patients presenting in status asthmaticus: Patients with a CAS of greater than or equal to 10 on presentation that have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival OR Patients with a CAS of greater than or equal to 10 that have not received treatment prior to arrival and after 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2 OR Patients with a CAS above 6 but less than 10 as measured 1 hour after initiation of standard treatment per AU's moderate asthma pathway Exclusion Criteria: Pregnancy Congestive Heart Failure or prior diagnosis of cardiovascular disease (congenital or acquired) Chronic lung disease outside of a previous diagnosis of Asthma Seizure disorder Liver disease History of hypertension greater than 95% for age Obstructive Sleep Apnea with AHI greater than 5 History of allergic or serious reaction to Ketamine Significant history of psychiatric illness defined as any patient with a diagnosis of psychiatric illness meeting the Diagnostic and Statistical Manual of Mental Disorders V criteria (severe Autism)
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Aimee E Baer Ellington, MD
    Phone
    770-354-2112
    Email
    abaerellington@augusta.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Lorna Bell, MD
    Phone
    7065332910
    Email
    lbell@augusta.edu

    12. IPD Sharing Statement

    Learn more about this trial

    The Role of Ketamine as an Adjuvant Therapy for Children With Acute Status Asthmaticus

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