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A Comparison of Two Doses of Intranasal Dexmedetomidine for Premedication in Children

Primary Purpose

Anxiety, Separation

Status
Unknown status
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
Dexmedetomidine
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety, Separation focused on measuring Sedation, dexmedetomidine, pediatric, preoperative period

Eligibility Criteria

6 Months - 5 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • All children of American Society of Anesthesiologists (ASA) physical status classification I or II (healthy) between the ages of 6 months and 5 years undergoing surgery at Queen Mary Hospital

Exclusion Criteria:

  • Any patient receiving other sedative premedication, allergy to dexmedetomidine, organ dysfunction, cardiac arrhythmia and congenital heart disease.

Sites / Locations

  • Queen Mary HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Dexmedetomidine 2 mcg/kg

Dexmedetomidine 4 mcg/kg

Arm Description

2 mcg/kg dexmedetomidine given intranasally once at least 30 minutes before anaesthetic induction

4 mcg/kg dexmedetomidine given intranasally once at least 30 minutes before anaesthetic induction

Outcomes

Primary Outcome Measures

Satisfactory sedation
The primary outcome will be the proportion of children with satisfactory sedation at the time of anaesthesic induction.

Secondary Outcome Measures

Time to satisfactory sedation
Time taken from drug administration to when the child's sedation level is that of only responding after mild prodding or shaking
Blood pressure
Blood pressure will be taken every 5 minutes
Heart rate
Heart rate will be taken every 5 minutes
Oxygen saturations
Oxygen saturations will be taken every 5 minutes

Full Information

First Posted
May 20, 2015
Last Updated
April 15, 2016
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT02459509
Brief Title
A Comparison of Two Doses of Intranasal Dexmedetomidine for Premedication in Children
Official Title
A Comparison of Two Doses of Intranasal Dexmedetomidine for Premedication in Children - a Double- Blind Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2015 (undefined)
Primary Completion Date
May 2016 (Anticipated)
Study Completion Date
May 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong

4. Oversight

5. Study Description

Brief Summary
The purpose of the study is to determine if 4mcg/kg of intranasal dexmedetomidine is better than 2mcg/kg in successfully sedating a child prior to induction of anesthesia.
Detailed Description
Dexmedetomidine is a selective alpha-2 adrenoreceptor agonist that has sedative, anxiolytic and analgesic properties without causing respiratory depression. It has been administered safely and effectively via a number of routes including as an intravenous infusion, intramuscularly, intranasally, buccally and orally . Yuen et al established that the median time of onset of sedation is 25-30 minutes, making it an ideal agent for preoperative sedation. The same group also studied doses of 1 mcg/kg and 2 mcg/kg as a sedative premedication and found that the success rates of appropriate sedation at induction in children aged 1 to 8 years were 53% and 66% respectively, with a dose related increase in successful sedation. Much higher doses of dexmedetomidine have also been used safely. Administered intravenously, 3mcg/kg of dexmedetomidine has been shown to provide satisfactory sedation for paediatric MRI in 97% of cases, without adverse effects. The investigators aim to show that high dose intranasal dexmedetomidine is a safe, effective and an easily administered sedative premedication. The investigators hypothesise that 4mcg/kg compared to 2mcg/kg of intranasal dexmedetomidine will lead to at least a 20% increase in the proportion of satisfactorily sedated patients at the time of anaesthesia induction. The primary outcome will be the proportion of children with satisfactory sedation at the time of anaesthesia induction. Suitable patients will be identified from the theatre lists and consent will be sought from their legal guardians during preassessment clinic or during their anaesthetic preoperative assessment on the ward. In a previous study, 66% of children aged 1-5 years were satisfactorily sedated at the time of induction with 2 mcg/kg of intranasal dexmedetomidine. In order to find a 20% difference with 4 mcg/kg of dexmedetomidine, the investigators' sample size needs to be 140 (70 in each group), for a power of 0.8 and a 5% false positive rate. The demographic data will be analysed by t test and chi-square test. The proportions of satisfactory sedation will be analysed by chi-square test. The onset sedation time and duration of sedation will be analysed by survival analysis. The vital signs over times will be expressed by percentage changes from baseline and estimated by mean and standard errors. A p-value<0.05 will be considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Separation
Keywords
Sedation, dexmedetomidine, pediatric, preoperative period

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dexmedetomidine 2 mcg/kg
Arm Type
Active Comparator
Arm Description
2 mcg/kg dexmedetomidine given intranasally once at least 30 minutes before anaesthetic induction
Arm Title
Dexmedetomidine 4 mcg/kg
Arm Type
Active Comparator
Arm Description
4 mcg/kg dexmedetomidine given intranasally once at least 30 minutes before anaesthetic induction
Intervention Type
Drug
Intervention Name(s)
Dexmedetomidine
Other Intervention Name(s)
Precedex
Intervention Description
Either 2mcg/kg or 4mcg/kg of intranasal dexmedetomidine will be given to assess efficacy of preoperative sedation
Primary Outcome Measure Information:
Title
Satisfactory sedation
Description
The primary outcome will be the proportion of children with satisfactory sedation at the time of anaesthesic induction.
Time Frame
From 30 minutes post drug administration to induction of anaesthesia (average 30 minutes)
Secondary Outcome Measure Information:
Title
Time to satisfactory sedation
Description
Time taken from drug administration to when the child's sedation level is that of only responding after mild prodding or shaking
Time Frame
From time of drug administration to when Observer's Assessment of Alertness/ Sedation Score is 2 or less (from 0 minutes to 30 minutes)
Title
Blood pressure
Description
Blood pressure will be taken every 5 minutes
Time Frame
From drug administration to end of anaesthesia (on average 1 to 3 hours)
Title
Heart rate
Description
Heart rate will be taken every 5 minutes
Time Frame
From drug administration to end of anaesthesia (on average 1 to 3 hours)
Title
Oxygen saturations
Description
Oxygen saturations will be taken every 5 minutes
Time Frame
From drug administration to end of anaesthesia (on average 1 to 3 hours)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All children of American Society of Anesthesiologists (ASA) physical status classification I or II (healthy) between the ages of 6 months and 5 years undergoing surgery at Queen Mary Hospital Exclusion Criteria: Any patient receiving other sedative premedication, allergy to dexmedetomidine, organ dysfunction, cardiac arrhythmia and congenital heart disease.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sophie E Liu, MBBS
Phone
852 55086630
Email
sophieliu@doctors.org.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Theresa Hui, MBBS
Phone
852 95368149
Email
huiwct@ha.org.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sophie E Liu, MBBS
Organizational Affiliation
Hong Kong University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sophie E Liu, MBBS
Phone
55086630
Email
sophieliu@doctors.org.uk
First Name & Middle Initial & Last Name & Degree
Theresa Hui, MBBS
Phone
95368149
Email
huiwct@ha.org.hk
First Name & Middle Initial & Last Name & Degree
Sophie E Liu, MBBS
First Name & Middle Initial & Last Name & Degree
Theresa Hui, MBBS
First Name & Middle Initial & Last Name & Degree
Grace Wong, MBBS
First Name & Middle Initial & Last Name & Degree
Vivian Yuen, MBBS
First Name & Middle Initial & Last Name & Degree
Michael G Irwin, MBChB
First Name & Middle Initial & Last Name & Degree
Silky Wong, MBBS

12. IPD Sharing Statement

Citations:
PubMed Identifier
21461792
Citation
Pestieau SR, Quezado ZM, Johnson YJ, Anderson JL, Cheng YI, McCarter RJ, Choi S, Finkel JC. High-dose dexmedetomidine increases the opioid-free interval and decreases opioid requirement after tonsillectomy in children. Can J Anaesth. 2011 Jun;58(6):540-50. doi: 10.1007/s12630-011-9493-7. Epub 2011 Apr 2.
Results Reference
result
PubMed Identifier
18363626
Citation
Mason KP, Zurakowski D, Zgleszewski SE, Robson CD, Carrier M, Hickey PR, Dinardo JA. High dose dexmedetomidine as the sole sedative for pediatric MRI. Paediatr Anaesth. 2008 May;18(5):403-11. doi: 10.1111/j.1460-9592.2008.02468.x. Epub 2008 Mar 18.
Results Reference
result
PubMed Identifier
21862817
Citation
Mason KP, Lubisch NB, Robinson F, Roskos R. Intramuscular dexmedetomidine sedation for pediatric MRI and CT. AJR Am J Roentgenol. 2011 Sep;197(3):720-5. doi: 10.2214/AJR.10.6134.
Results Reference
result
PubMed Identifier
17646493
Citation
Yuen VM, Irwin MG, Hui TW, Yuen MK, Lee LH. A double-blind, crossover assessment of the sedative and analgesic effects of intranasal dexmedetomidine. Anesth Analg. 2007 Aug;105(2):374-80. doi: 10.1213/01.ane.0000269488.06546.7c.
Results Reference
result
PubMed Identifier
22950484
Citation
Yuen VM, Hui TW, Irwin MG, Yao TJ, Chan L, Wong GL, Shahnaz Hasan M, Shariffuddin II. A randomised comparison of two intranasal dexmedetomidine doses for premedication in children. Anaesthesia. 2012 Nov;67(11):1210-6. doi: 10.1111/j.1365-2044.2012.07309.x. Epub 2012 Sep 5.
Results Reference
result

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A Comparison of Two Doses of Intranasal Dexmedetomidine for Premedication in Children

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