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Trial registered on ANZCTR
Registration number
ACTRN12613000313730
Ethics application status
Approved
Date submitted
19/03/2013
Date registered
20/03/2013
Date last updated
15/04/2015
Type of registration
Retrospectively registered
Titles & IDs
Public title
Self controlled trial of Ambu Ascope for training clinicians in fibreoptic device guided intubation
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Scientific title
An evaluation of the Ambu Ascope for training clinicians in fibreoptic device guided orotracheal intubation as assessed using a Global Rating Scale
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Secondary ID [1]
282117
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Nil
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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:
Airway management
288610
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Condition category
Condition code
Anaesthesiology
288943
288943
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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
Ascope assisted orotracheal intubations will be performed on anaesthetised patients
Operators given set of 5 Ascopes - operators are composed of 5 consultant anaesthetists and 3 anaesthesia registrars
1st to 5th attempt will be recorded on notebook PC. All attempts are carried out on different patients.
Ascope will be used for each attempt
GRS score evaluated on recordings
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Intervention code [1]
286720
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Treatment: Devices
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Comparator / control treatment
Nil
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
289071
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GRS score - Global Rating Scale - score of 1-5 to define bronchoscopic efficacy
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Assessment method [1]
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Timepoint [1]
289071
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during performance of Ascope assisted intubation
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Secondary outcome [1]
301675
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intubation success
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Assessment method [1]
301675
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Timepoint [1]
301675
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during performance of Ascope assisted intubation
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Secondary outcome [2]
301857
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intubation time
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Assessment method [2]
301857
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Timepoint [2]
301857
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during performance of Ascope assisted intubation
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Eligibility
Key inclusion criteria
able to consent for themselves
general anaesthesia
orotracheal intubation
ASA I-III
fasted for surgery
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Minimum age
18
Years
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Maximum age
85
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
patients with indication for awake FOI
inhalational induction
known difficult/ impossible mask ventilation
rapid sequence induction
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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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
1/04/2013
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Actual
12/03/2013
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Date of last participant enrolment
Anticipated
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Actual
21/11/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
735
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The Northern Hospital - Epping
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Recruitment postcode(s) [1]
6534
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3076 - Epping
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Funding & Sponsors
Funding source category [1]
286882
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Hospital
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Name [1]
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The Northern Hospital
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Address [1]
286882
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185 Cooper St
Epping
Victoria 3076
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Country [1]
286882
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Australia
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Funding source category [2]
286883
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Commercial sector/Industry
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Name [2]
286883
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Ambu Australia
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Address [2]
286883
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Ambu Australia Pty. Ltd. - Office
2401/4 Daydream St.
NSW 2102
Warriewood
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Country [2]
286883
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Australia
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Primary sponsor type
Hospital
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Name
The Northern Hospital
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Address
185 Cooper St
Epping
Victoria 3076
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Country
Australia
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Secondary sponsor category [1]
285673
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None
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Name [1]
285673
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Address [1]
285673
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Country [1]
285673
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
288975
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Northern Health HREC
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Ethics committee address [1]
288975
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Northern Hospital 185 Cooper St Epping Vic 3076
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Ethics committee country [1]
288975
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Australia
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Date submitted for ethics approval [1]
288975
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Approval date [1]
288975
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27/11/2012
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Ethics approval number [1]
288975
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P17/12
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Summary
Brief summary
This research is designed specifically to compare the performance before and after exposure to the Ambu Ascope in the clinical setting for scope guided intubation. Endpoints will be GRS score, success in intubation and time taken for intubation on the first and 5th attempts with Ascope. The null hypothesis for this research project is that there is no difference in GRS score before and after 5 attempts with Ambu Ascope
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Trial website
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Trial related presentations / publications
none
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Public notes
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Contacts
Principal investigator
Name
38454
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Dr Jun Keat Chan
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Address
38454
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Department of Anaesthesia and Pain Management
Northern Hospital
185 Cooper St
Epping
Vic 3076
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Country
38454
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Australia
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Phone
38454
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+61384058000
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Fax
38454
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Email
38454
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[email protected]
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Contact person for public queries
Name
38455
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Jun Keat Chan
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Address
38455
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Department of Anaesthesia and Pain Management
Northern Hospital
185 Cooper St
Epping
Vic 3076
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Country
38455
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Australia
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Phone
38455
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+61384058000
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Fax
38455
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Email
38455
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[email protected]
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Contact person for scientific queries
Name
38456
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Jun Keat Chan
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Address
38456
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Department of Anaesthesia and Pain Management
Northern Hospital
185 Cooper St
Epping
Vic 3076
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Country
38456
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Australia
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Phone
38456
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+61384058000
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Fax
38456
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Email
38456
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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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