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Trial registered on ANZCTR
Registration number
ACTRN12606000121561
Ethics application status
Approved
Date submitted
4/04/2006
Date registered
4/04/2006
Date last updated
4/04/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
EMLA versus N2O for analgesia during intravenous cannulation of children in the emergency department
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Scientific title
A randomised clinical trial to compare the efficacy of Eutectic Mixture of Local Anaesthetics (EMLA) and nitrous oxide (N2O) in decreasing the pain of intravenous cannulation in children
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pain
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Condition category
Condition code
Anaesthesiology
1166
1166
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0
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Anaesthetics
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The study participants were randomised to receive EMLA (administered to the skin as standard EMLA patches for a duration of 45 minutes).
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Intervention code [1]
967
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None
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Comparator / control treatment
The study participants were randomised to receive nitrous oxide (administered as a 70%N2O/30%oxygen mixture via a face mask or mouthpiece for 3 minutes)
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Control group
Active
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Outcomes
Primary outcome [1]
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Child pain score
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Assessment method [1]
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Timepoint [1]
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Measured immediatley after the cannulation
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Secondary outcome [1]
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1. parental satisfaction score.
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Assessment method [1]
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Timepoint [1]
2846
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Measured immediately after cannulation of the child.
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Secondary outcome [2]
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2. adverse event rates.
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Assessment method [2]
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Timepoint [2]
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Measured immediately after cannulation of the child.
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Eligibility
Key inclusion criteria
Required IV cannulation or venepuncture.
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Minimum age
3
Years
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Maximum age
15
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
They were excluded if allergy to EMLA or nitrous oxide, suspected pneumothorax, bowel obstruction or other trapped gas, or if the parent/guardian are non-English speaking. Patients also need to be able to wait at least thirty minutes prior to cannulation.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
A note containing each individual patients allocation was sealed in an envelope inside each study pack
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated random numbers
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/03/2005
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Northern Hospital (Victoria)
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Address [1]
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Country [1]
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Primary sponsor type
Hospital
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Name
Northern Hospital, VIC
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Address
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Country
Australia
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Austin Hospital, VIC
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Address [1]
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Northern Hospital
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
2607
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Approval date [1]
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24/05/2005
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Ethics approval number [1]
2607
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09/05
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Summary
Brief summary
IV cannulation can be painful. Both EMLA and nitrous oxide can be used for analgesia, especially in children. We aimed to determine which is better for pain relief in children for this procedure
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Associate Professor David Taylor
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Address
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Emergency Department
Austin Hospital
Studley Road
Heidelberg VIC 3084
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Country
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Australia
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Phone
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+61 3 94964883
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Fax
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+61 3 94963380
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Timothy Mann
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Address
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Emergency Department
The Northern Hospital
195 Cooper Street
Epping VIC 3076
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Country
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Australia
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Phone
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+61 3 84058000
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Fax
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+61 3 84058524
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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