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Trial registered on ANZCTR
Registration number
ACTRN12609000236291
Ethics application status
Approved
Date submitted
21/07/2007
Date registered
11/05/2009
Date last updated
16/08/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
Randomised trial comparing controlled oxygen therapy with high-flow oxygen therapy in the treatment of patients with Acute Exacerbations of Chronic Obstructive Pulmonary Disease (AECOPD) in the pre-hospital setting
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Scientific title
Randomised trial comparing controlled oxygen therapy with high-flow oxygen therapy in the treatment of patients with Acute Exacerbations of Chronic Obstructive Pulmonary Disease (AECOPD) in the pre-hospital setting
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Secondary ID [1]
262847
0
none
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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:
Chronic Obstructive Pulmonary Disease (COPD)
2180
0
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Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD)
4652
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Condition category
Condition code
Respiratory
2275
2275
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0
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Chronic obstructive pulmonary disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
controlled oxygen therapy to maintain oxygen saturations between 88-92% using nasal prongs and mask oxygen with nebulization of medication done by handheld air driven compressor for the duration of the ambulance transport once off treatment pre hospitally
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Intervention code [1]
1900
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Treatment: Other
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Comparator / control treatment
High Flow oxygen therapy- provide high concentration of oxygen 8-10 L/min by Non re-breather mask and all nebulized medication will be driven by 6-8L oxygen for the duration of the transport by ambulance.
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Control group
Active
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Outcomes
Primary outcome [1]
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Mortality, death in hospital post treatment by ambulance offerers for AECOPD, or death during the care of ambulance officers
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Assessment method [1]
5803
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Timepoint [1]
5803
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Mortality during hospital stay after transport by ambulance and treated for AECOPD, during this episode only
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Secondary outcome [1]
5276
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ventilation - invasive and non invasive required during treatment by Ambulance officers of during stay in hospital after treated pre-hospitally for AECOPD
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Assessment method [1]
5276
0
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Timepoint [1]
5276
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ventilation required during transport or duing hospital admission after transport by Ambulance officers and treated for AECOPD
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Secondary outcome [2]
5277
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arterial blood gas (ABG) results assess within 30 min of arrival after treatment by ambulance for AECOPD
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Assessment method [2]
5277
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Timepoint [2]
5277
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Hospital admission within 30min of arrival
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Secondary outcome [3]
241804
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Length of Hospital Stay
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Assessment method [3]
241804
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Timepoint [3]
241804
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after treatment for AECOPD by ambulance officers the length of hospital stay during this admission measured in days
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Eligibility
Key inclusion criteria
Confirmed Diagnosis COPD, acute respiratory symptoms, Transport and treatment by Tasmanian Ambulance Staff
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Minimum age
35
Years
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Maximum age
No limit
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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
Asthma patients
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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)
Signed consent forms were received. A list of consenting paramedics was compiled, with city and rural area staff listed separately. Staff were listed in the order in which consent forms were received and then randomly assigned to the treatment groups using the random number generator feature in Microsoft Excel. Staff with odd numbers were assigned to the controlled oxygen therapy treatment group and those with even numbers were assigned to the high flow oxygen therapy treatment group. Paramedics were instructed to follow the protocol for the oxygen therapy treatment group to which they were assigned during shifts where they were the designated treating officer. Randomization by officer no concealment.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Staff were listed in the order in which consent forms were received and then randomly assigned to the treatment groups using the random number generator feature in Microsoft Excel.
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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
Phase 1
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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
1/07/2006
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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
150
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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]
2440
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Other Collaborative groups
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Name [1]
2440
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Australian College for Ambulance Professionals
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Address [1]
2440
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1 Mellvile Street
Hobart Tasmania 7000
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Country [1]
2440
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Australia
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Funding source category [2]
4833
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University
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Name [2]
4833
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University of Tasmania (UTAS)
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Address [2]
4833
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UTAS
Clinical School, Private Bag 99
Hobart Tasmania
7001
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Country [2]
4833
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Australia
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Funding source category [3]
4834
0
Self funded/Unfunded
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Name [3]
4834
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Dr Michael Austin
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Address [3]
4834
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Menzies
Private bag 23
Hobart Tasmania 7001
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Country [3]
4834
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Australia
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Primary sponsor type
Individual
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Name
Associate Professor Richard Wood-Baker
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Address
Menzies
Private bag 23
Hobart Tasmania 7001
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Country
Australia
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Secondary sponsor category [1]
4374
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None
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Name [1]
4374
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Address [1]
4374
0
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Country [1]
4374
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
4290
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Human Research Ethics Committee of Tasmania
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Ethics committee address [1]
4290
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Ethics committee country [1]
4290
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Australia
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Date submitted for ethics approval [1]
4290
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Approval date [1]
4290
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Ethics approval number [1]
4290
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Summary
Brief summary
Purpose to determine if different oxygen therapies for patients having AECOPD in the pre-hospital setting have different outcomes (ie. Mortality, length of hospital stay, requirement for ventilation, difference ABGs)
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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
27714
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Country
27714
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Phone
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Fax
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Email
27714
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Contact person for public queries
Name
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Mr. Michael A Austin
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Address
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Department of Respiratory Medicine
Royal Hobart Hospital
Liverpool Street
Hobart TAS 7000
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Country
11089
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Australia
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Phone
11089
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+61 3 6226 7778
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Fax
11089
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Email
11089
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[email protected]
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Contact person for scientific queries
Name
2017
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Dr. Michael A Austin
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Address
2017
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Department of Respiratory Medicine, Menzies Research Institute
Macquarie Street
Royal Hobart Hospital
Hobart TAS 7000
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Country
2017
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Australia
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Phone
2017
0
+61 3 6226 7778
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Fax
2017
0
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Email
2017
0
[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
Source
Title
Year of Publication
DOI
Dimensions AI
Effect of high flow oxygen on mortality in chronic obstructive pulmonary disease patients in prehospital setting: randomised controlled trial
2010
https://doi.org/10.1136/bmj.c5462
N.B. These documents automatically identified may not have been verified by the study sponsor.
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