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Intranasal Ketamine for Anxiolysis in Pediatric Emergency Department Patients

Primary Purpose

Anxiety, Pediatric ALL, Procedural Anxiety

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ketamine 100 MG/ML
Midazolam 5 MG/ML
Sponsored by
Brooke Army Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety

Eligibility Criteria

2 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients age 2 to 12 years who present to the ED
  • Requiring intravenous access
  • Requiring laceration repairs
  • Requiring incision and drainage of abscesses
  • Requiring digital nerve blocks
  • Requiring radiological imaging
  • Requiring bladder catheterization
  • Requiring foreign body removal.

Exclusion Criteria:

  • Vital sign abnormalities greater than 20% deviation from age-normalized ranges
  • Altered mental status/delirium or intoxication
  • Patient or patient's parent/guardian are unwilling to participate or provide informed consent
  • Any allergy to ketamine or midazolam
  • Patient is female with history of menarche
  • Presence of chronic oxygen-dependent pulmonary disease, liver cirrhosis, or renal disease requiring dialysis
  • Presence of ischemic heart disease, heart failure, or a history of unstable dysrhythmias
  • Presence of intracranial mass or vascular lesion.
  • Presence of a history of psychosis or hallucinations
  • Weight greater than 100kg
  • History of increased intracranial pressure/ hypertensive hydrocephalus within the last 3 months
  • Non-English speaking/reading parent/guardian and/or patients
  • Patient is acutely psychotic
  • Provider feels that patient currently or likely will require chemical and/or physical restraints
  • History of prolonged QT-interval
  • Nasal trauma
  • Epistaxis

Sites / Locations

  • San Antonio Military Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ketamine

Midazolam

Arm Description

Ketamine 100 mg/mL concentration administered in a single 1.0 mg/kg dose with a maximum of 50mg intranasal via mucosal atomization device.

Midazolam 5 mg/mL concentration administered in a single administered in a single 0.3 mg/kg dose with a maximum of 5mg intranasal via mucosal atomization device.

Outcomes

Primary Outcome Measures

Change in mYPAS
Modified Yale preoperative anxiety scale

Secondary Outcome Measures

Change in sedation scale
University of Michigan sedation scale
Change in pain rating (Wong-Baker Pain Faces Rating Scale)
Wong-Baker Pain Faces Rating Scale
Change in anxiety score (Visual analogue scale)
Visual analogue scale

Full Information

First Posted
January 30, 2017
Last Updated
April 23, 2023
Sponsor
Brooke Army Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03043430
Brief Title
Intranasal Ketamine for Anxiolysis in Pediatric Emergency Department Patients
Official Title
Anxiolysis for Emergency Department Procedures in Pediatric Patients Using Intranasal Ketamine Compared With Intranasal Midazolam: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Terminated
Why Stopped
Research manpower shortage
Study Start Date
May 2016 (Actual)
Primary Completion Date
April 2023 (Actual)
Study Completion Date
April 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brooke Army Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Investigators plan to conduct a randomized, double-blinded, controlled study among pediatric patients requiring minor procedures in the Emergency Department setting. Patients will be randomized to one of two arms of intranasal treatments: ketamine 1.0 mg/kg (K) or midazolam 0.3 mg/kg (M). The primary outcome will be change in anxiety using the Modified Yale Preoperative Anxiety Scale (mYPAS).
Detailed Description
The intranasal route of drug delivery is commonly used in Emergency Departments (ED) in pediatric patients. Multiple trials have shown the safety of administration of intranasal ketamine, including studies performed in the ED to treat pain in pediatric patients. The use of ketamine for anxiolysis has not been directly studied; however, ketamine has been shown to have anxiolytic effect at low doses as secondary outcomes when studied. Midazolam has been established as an effective medication to provide analgesia and anxiolysis. Investigators plan to conduct a randomized, double-blinded, controlled study in the Emergency Department. Pediatric patients presenting to the ED with the need for minor procedures who meet the inclusion and exclusion criteria will be consented, and if amenable, will be enrolled. Patients will be randomized to one of two arms of intranasal treatments: ketamine 1.0 mg/kg (K) or midazolam 0.3 mg/kg (M). Patients will be tracked for symptom improvement within the Emergency Department. The primary outcome will be change in anxiety from initial measurement to measurement 5 minutes pre-procedure using the Modified Yale Preoperative Anxiety Scale (mYPAS). Secondary outcomes will include sedation level, adverse events, need for additional medications, change in pain rating, patient and/or parent/guardian satisfaction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Pediatric ALL, Procedural Anxiety

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Subjects will be randomized to one of two treatment arms.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Medication (ketamine versus midazolam) will be drawn up in unmarked syringe and applied to the patient by mucosal atomization device by a nurse not directly involved in the investigation or the patient's care.
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ketamine
Arm Type
Experimental
Arm Description
Ketamine 100 mg/mL concentration administered in a single 1.0 mg/kg dose with a maximum of 50mg intranasal via mucosal atomization device.
Arm Title
Midazolam
Arm Type
Active Comparator
Arm Description
Midazolam 5 mg/mL concentration administered in a single administered in a single 0.3 mg/kg dose with a maximum of 5mg intranasal via mucosal atomization device.
Intervention Type
Drug
Intervention Name(s)
Ketamine 100 MG/ML
Intervention Description
Administer ketamine via mucosal atomization device
Intervention Type
Drug
Intervention Name(s)
Midazolam 5 MG/ML
Intervention Description
Administer midazolam via mucosal atomization device
Primary Outcome Measure Information:
Title
Change in mYPAS
Description
Modified Yale preoperative anxiety scale
Time Frame
Change in score between initial measurement versus 5 minutes pre-procedure
Secondary Outcome Measure Information:
Title
Change in sedation scale
Description
University of Michigan sedation scale
Time Frame
Change in score between initial measurement versus 5 minutes pre procedure, 5 minutes post procedure, and 5 minutes pre-discharge
Title
Change in pain rating (Wong-Baker Pain Faces Rating Scale)
Description
Wong-Baker Pain Faces Rating Scale
Time Frame
Change in score between initial measurement versus 5 minutes pre procedure, 5 minutes post procedure, and 5 minutes pre-discharge
Title
Change in anxiety score (Visual analogue scale)
Description
Visual analogue scale
Time Frame
Change in score between initial measurement versus 5 minutes pre procedure, 5 minutes post procedure, and 5 minutes pre-discharge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients age 2 to 12 years who present to the ED Requiring intravenous access Requiring laceration repairs Requiring incision and drainage of abscesses Requiring digital nerve blocks Requiring radiological imaging Requiring bladder catheterization Requiring foreign body removal. Exclusion Criteria: Vital sign abnormalities greater than 20% deviation from age-normalized ranges Altered mental status/delirium or intoxication Patient or patient's parent/guardian are unwilling to participate or provide informed consent Any allergy to ketamine or midazolam Patient is female with history of menarche Presence of chronic oxygen-dependent pulmonary disease, liver cirrhosis, or renal disease requiring dialysis Presence of ischemic heart disease, heart failure, or a history of unstable dysrhythmias Presence of intracranial mass or vascular lesion. Presence of a history of psychosis or hallucinations Weight greater than 100kg History of increased intracranial pressure/ hypertensive hydrocephalus within the last 3 months Non-English speaking/reading parent/guardian and/or patients Patient is acutely psychotic Provider feels that patient currently or likely will require chemical and/or physical restraints History of prolonged QT-interval Nasal trauma Epistaxis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nadia M Pearson, MD
Organizational Affiliation
Faculty Physician
Official's Role
Principal Investigator
Facility Information:
Facility Name
San Antonio Military Medical Center
City
Fort Sam Houston
State/Province
Texas
ZIP/Postal Code
78234
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22688444
Citation
Hosseini Jahromi SA, Hosseini Valami SM, Adeli N, Yazdi Z. Comparison of the effects of intranasal midazolam versus different doses of intranasal ketamine on reducing preoperative pediatric anxiety: a prospective randomized clinical trial. J Anesth. 2012 Dec;26(6):878-82. doi: 10.1007/s00540-012-1422-6. Epub 2012 Jun 12.
Results Reference
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PubMed Identifier
15675259
Citation
Roelofse JA, Shipton EA, de la Harpe CJ, Blignaut RJ. Intranasal sufentanil/midazolam versus ketamine/midazolam for analgesia/sedation in the pediatric population prior to undergoing multiple dental extractions under general anesthesia: a prospective, double-blind, randomized comparison. Anesth Prog. 2004;51(4):114-21.
Results Reference
background
PubMed Identifier
26417129
Citation
Narendra PL, Naphade RW, Nallamilli S, Mohd S. A comparison of intranasal ketamine and intranasal midazolam for pediatric premedication. Anesth Essays Res. 2015 May-Aug;9(2):213-8. doi: 10.4103/0259-1162.154051.
Results Reference
background
PubMed Identifier
24665234
Citation
Khatavkar SS, Bakhshi RG. Comparison of nasal Midazolam with Ketamine versus nasal Midazolam as a premedication in children. Saudi J Anaesth. 2014 Jan;8(1):17-21. doi: 10.4103/1658-354X.125904.
Results Reference
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Intranasal Ketamine for Anxiolysis in Pediatric Emergency Department Patients

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