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Volumes of Administration for Intranasal Midazolam

Primary Purpose

Children Requiring Sedation to Facilitate Laceration Repair

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Intranasal midazolam
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Children Requiring Sedation to Facilitate Laceration Repair focused on measuring Sedation, Laceration repair, Children, Intranasal, Midazolam

Eligibility Criteria

1 Year - 7 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1 to 7 years of age, inclusive.
  • Require intranasal midazolam for minimal sedation to facilitate laceration repair.

Exclusion Criteria:

  • Weight less than 10 kg.
  • Known allergy to midazolam.
  • Presence of intranasal obstruction (e.g. mucous or blood) that cannot be readily cleared
  • Inability to speak English or Spanish
  • Developmental delay, psychiatric illness, neurologic impairment, or altered mental status; or illnesses associated with chronic pain (e.g. sickle cell disease, inflammatory bowel disease).
  • Foster children or wards.

Sites / Locations

  • New York Presbyterian Morgan Stanley Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

200 mcL VOA

500 mcL VOA

1000 mcL VOA

Arm Description

Intranasal midazolam administered in 200 mcL VOA

Intranasal midazolam administered in 500 mcL VOA.

Intranasal midazolam administered in 1000 mcL VOA.

Outcomes

Primary Outcome Measures

Median Time (Minutes) After Administration of Intranasal Midazolam Until Patient Achieves Minimal Sedation
This outcome is designed to examine time to onset of minimal sedation, defined as a University of Michigan Sedation Score (UMSS) of 1.

Secondary Outcome Measures

Observational Scale of Behavioral Distress - Revised
The Observational Scale of Behavioral Distress - revised (OSBD-r) is an eight-factor, weighted observational scale used to measure distress associated with medical procedures in children 1 to 20 years of age. The total OSBD-r score is the sum of the OSBD-r scores for predetermined clinically relevant phases of the procedure, with each phase assigned a score from 0 to 23.5 (0=no distress, 23.5=maximum distress), based on the frequency and types of behaviors observed during a pre-determined number of 15-second intervals during each phase.
Number of Patients With Physicians Who Were Satisfied or Very Satisfied With Ease of Medication Administration
This outcome is designed to examine MD satisfaction with ease of administration of intranasal medication - physicians who expressed that they were satisfied or very satisfied with ease of medication administration will be counted.

Full Information

First Posted
June 29, 2013
Last Updated
April 17, 2019
Sponsor
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT01948908
Brief Title
Volumes of Administration for Intranasal Midazolam
Official Title
Optimal Volumes of Administration for Intranasal Midazolam in Children
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine exactly how much drug volume should be administered into each nare, so that the drug absorption can be maximized and the amount that runs out of the nose, or is swallowed, is minimized, thereby optimizing the effectiveness of any drug given intranasally. The investigators will determine this ideal "volume of administration" by studying intranasal midazolam in children who require sedation to facilitate laceration repairs. The investigators will evaluate both clinical outcomes as well as pharmacokinetic outcomes associated with each volume of administration. We will block randomize children to receive intranasal midazolam in maximum aliquots of one of the three following VOA: 200 microliters (mcL), 500 mcL, or 1000 mcL.
Detailed Description
The intranasal route is an effective means of administering sedative medications for children. However, sometimes the child has to receive a certain dose that requires a very large volume to be administered into the nose, because of the types of concentrations of drugs that are available. Most drugs are not concentrated enough so that small volumes can be consistently given, so as a result, sometimes a very large amount of medication is administered intranasally. When the amount is too large, most of the medication either runs back out the nose, or down the back of the nose and throat and is swallowed, instead of being absorbed in the nasal cavity, where it can be quickly absorbed and produce optimal effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Children Requiring Sedation to Facilitate Laceration Repair
Keywords
Sedation, Laceration repair, Children, Intranasal, Midazolam

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
99 (Actual)

8. Arms, Groups, and Interventions

Arm Title
200 mcL VOA
Arm Type
Experimental
Arm Description
Intranasal midazolam administered in 200 mcL VOA
Arm Title
500 mcL VOA
Arm Type
Experimental
Arm Description
Intranasal midazolam administered in 500 mcL VOA.
Arm Title
1000 mcL VOA
Arm Type
Experimental
Arm Description
Intranasal midazolam administered in 1000 mcL VOA.
Intervention Type
Drug
Intervention Name(s)
Intranasal midazolam
Other Intervention Name(s)
No other name
Intervention Description
Intranasal midazolam, 0.5 mg/kg, maximum dose 10 mg, administered using mucosal atomization device (MAD).
Primary Outcome Measure Information:
Title
Median Time (Minutes) After Administration of Intranasal Midazolam Until Patient Achieves Minimal Sedation
Description
This outcome is designed to examine time to onset of minimal sedation, defined as a University of Michigan Sedation Score (UMSS) of 1.
Time Frame
20 minutes
Secondary Outcome Measure Information:
Title
Observational Scale of Behavioral Distress - Revised
Description
The Observational Scale of Behavioral Distress - revised (OSBD-r) is an eight-factor, weighted observational scale used to measure distress associated with medical procedures in children 1 to 20 years of age. The total OSBD-r score is the sum of the OSBD-r scores for predetermined clinically relevant phases of the procedure, with each phase assigned a score from 0 to 23.5 (0=no distress, 23.5=maximum distress), based on the frequency and types of behaviors observed during a pre-determined number of 15-second intervals during each phase.
Time Frame
60 minutes
Title
Number of Patients With Physicians Who Were Satisfied or Very Satisfied With Ease of Medication Administration
Description
This outcome is designed to examine MD satisfaction with ease of administration of intranasal medication - physicians who expressed that they were satisfied or very satisfied with ease of medication administration will be counted.
Time Frame
60 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1 to 7 years of age, inclusive. Require intranasal midazolam for minimal sedation to facilitate laceration repair. Exclusion Criteria: Weight less than 10 kg. Known allergy to midazolam. Presence of intranasal obstruction (e.g. mucous or blood) that cannot be readily cleared Inability to speak English or Spanish Developmental delay, psychiatric illness, neurologic impairment, or altered mental status; or illnesses associated with chronic pain (e.g. sickle cell disease, inflammatory bowel disease). Foster children or wards.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel S Tsze, MD, MPH
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York Presbyterian Morgan Stanley Children's Hospital
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27823876
Citation
Tsze DS, Ieni M, Fenster DB, Babineau J, Kriger J, Levin B, Dayan PS. Optimal Volume of Administration of Intranasal Midazolam in Children: A Randomized Clinical Trial. Ann Emerg Med. 2017 May;69(5):600-609. doi: 10.1016/j.annemergmed.2016.08.450. Epub 2016 Nov 4.
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Volumes of Administration for Intranasal Midazolam

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