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Trial registered on ANZCTR
Registration number
ACTRN12605000673640
Ethics application status
Approved
Date submitted
9/08/2005
Date registered
21/10/2005
Date last updated
7/11/2018
Date data sharing statement initially provided
7/11/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Study of Overnight Humidification for Children with Tracheostomies
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Scientific title
Study of Overnight Humidification for Children with Tracheostomies: A crossover study comparing the effects of a heated humidifier vs a heat and moisture exchanger on mucus viscoelasticity
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Secondary ID [1]
199
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Auckland District Health Board: A+3190
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Secondary ID [2]
200
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NTY/05/08/062
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Universal Trial Number (UTN)
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Trial acronym
Overnight HCT Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Children with tracheostomies
821
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Condition category
Condition code
Respiratory
885
885
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0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Heated Humidifier VS Heat and moisture exchanger (HME)
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Intervention code [1]
136
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Treatment: Devices
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
1148
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Mucus visocelasticity
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Assessment method [1]
1148
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Timepoint [1]
1148
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After 2 hours and 20 hours of treatment
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Secondary outcome [1]
2112
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Requirement for suctioning overnight.
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Assessment method [1]
2112
0
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Timepoint [1]
2112
0
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Eligibility
Key inclusion criteria
Children with tracheostomies in situ, Currently in patient, Have had at least one tracheostomy change.
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Minimum age
Not stated
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Maximum age
18
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
Heated humidification or HME not tolerated in the past, Thick airway secretions or other contraindication to stopping heated humidification, Known Cystic Fibrosis (CF), Known Primary Ciliary Dyskinesia (PCD), Known Primary immune deficiency.
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Study design
Purpose of the study
Treatment
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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)
Sealed Envelope
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated by website www.randomization.com, no blocking or stratification
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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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
1/09/2005
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Actual
26/11/2004
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Date of last participant enrolment
Anticipated
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Actual
31/01/2007
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Date of last data collection
Anticipated
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Actual
31/01/2007
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Sample size
Target
16
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Accrual to date
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Final
12
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Recruitment outside Australia
Country [1]
134
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New Zealand
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State/province [1]
134
0
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Funding & Sponsors
Funding source category [1]
976
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Commercial sector/Industry
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Name [1]
976
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Fisher and Paykel Healthcare,
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Address [1]
976
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Country [1]
976
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New Zealand
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Funding source category [2]
977
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Charities/Societies/Foundations
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Name [2]
977
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Foundation For Research Science and Technology
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Address [2]
977
0
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Country [2]
977
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New Zealand
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Primary sponsor type
Commercial sector/Industry
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Name
Fisher and Paykel Healthcare
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Address
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Country
New Zealand
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Secondary sponsor category [1]
843
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University
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Name [1]
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Uniservices, Univeristy of Auckland
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Address [1]
843
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Country [1]
843
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
2287
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Starship Hospital, ADHB
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Ethics committee address [1]
2287
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Ethics committee country [1]
2287
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Australia
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Date submitted for ethics approval [1]
2287
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Approval date [1]
2287
0
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Ethics approval number [1]
2287
0
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Summary
Brief summary
Introduction: This study is an observer-blinded cross-over study that aims to compare the short-term effects of two different forms of humidification of inspired gases for children with tracheostomies. The study compares the use of a Heated Humidifier to the use of a Heat and Moisture Exchanger (HME or Swedish nose) in providing humidification of the gases that children with tracheostomies breathe. The study will take place during the time period that children are admitted to the hospital following performance of a tracheostomy. These children are generally well during this period and are admitted while their parents are being trained in the care of a child with a tracheostomy and it is safe for them to go home. Each child will receive each form of humidification for a 20 hour period. There will be a one night interval and then the child will cross-over and receive the alternate form of humidification for a second 20 hour period. Assessment will be at the baseline for each period, after 2 hours of treatment and after 20 hours of treatment. Assessment will include suctioning of airway secretions for bacterial culture, mucus viscoelasticity, levels of inflammatory markers in airway secretions, oxygen saturation, and clinical examination plus any adverse events or failure to tolerate treatment.
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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
35670
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Dr David McNamara
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Address
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Paediatric Respiratory and Sleep Medicine
Starship Children's Hospital
1 Park Road
Grafton,
Auckland 1074
New Zealand
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Country
35670
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New Zealand
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Phone
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+64 93797440
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
9325
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Dr David McNamara
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Address
9325
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Department of Paediatrics
Univeristy of Auckland
Private Bag 92019
Auckland 1020
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Country
9325
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New Zealand
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Phone
9325
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+64 9 3737999
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Fax
9325
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Email
9325
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[email protected]
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Contact person for scientific queries
Name
253
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Dr David McNamara
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Address
253
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Department of Paediatrics
Univeristy of Auckland
Private Bag 92019
Auckland 1020
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Country
253
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New Zealand
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Phone
253
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+64 9 3737999
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Fax
253
0
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Email
253
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Not approved by local ethics committee
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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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