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Trial registered on ANZCTR
Registration number
ACTRN12606000429550
Ethics application status
Approved
Date submitted
28/09/2006
Date registered
4/10/2006
Date last updated
4/10/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Randomised comparison of the Ambu® Laryngeal Mask with the Laryngeal Mask Airway UniqueTM during anaesthesia in spontaneously breathing adult patients
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Scientific title
A single-blind randomised phase IV study to evaluate the effectiveness of the AMBU Aura-once disposable Laryngeal Mask against the Laryngeal Mask Airway -unique wih respect to sealing pressure and ease of use for airway maintenance during spontaneous ventilation general anaesthesia
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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 maintenance during anaesthesia
1401
0
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Condition category
Condition code
Anaesthesiology
1493
1493
0
0
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Other anaesthesiology
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Respiratory
1494
1494
0
0
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
AMBU laryngeal mask over the course of a single general anaesthetic procedure and 24 hrs post-operatively
Laryngeal Mask Airway - Unique over the course of a single general anaesthetic procedure and 24 hrs post-operatively
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Intervention code [1]
1381
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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]
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Airway leakage pressure
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Assessment method [1]
2064
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Timepoint [1]
2064
0
Measured just post device insertion
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Secondary outcome [1]
3555
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Time for insertion of device
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Assessment method [1]
3555
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Timepoint [1]
3555
0
As device is inserted
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Secondary outcome [2]
3556
0
Adequacy of airway post insertion
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Assessment method [2]
3556
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Timepoint [2]
3556
0
Throughout the surgical procedure
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Secondary outcome [3]
3557
0
Post operative sore throat
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Assessment method [3]
3557
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Timepoint [3]
3557
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Immediately post surgery, 24 hrs post surgery
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Eligibility
Key inclusion criteria
Adults who are undergoing general anaesthesia suitable for a LMA.
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Minimum age
18
Years
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Maximum age
Not stated
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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
Recognised non suitability for supraglottic airway usage.
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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)
Unaware of timing and group due to allocation being involved contacting the holder of the allocation schedule who was “off-site” or at central administration
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by using a randomization table created by a computer software.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
Patient is blinded to the intervention
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Phase
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
28/09/2006
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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
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]
1631
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Hospital
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Name [1]
1631
0
Royal Melbourne hospital
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Address [1]
1631
0
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Country [1]
1631
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Australia
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Primary sponsor type
Hospital
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Name
Royal Melbourne Hospital - Department of Anaesthesia and Pain Management
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Address
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Country
Australia
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Secondary sponsor category [1]
1434
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None
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Name [1]
1434
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Nil
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Address [1]
1434
0
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Country [1]
1434
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
3077
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Melbourne Health-Royal Melbourne Hospital
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Ethics committee address [1]
3077
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Ethics committee country [1]
3077
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Australia
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Date submitted for ethics approval [1]
3077
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Approval date [1]
3077
0
13/09/2006
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Ethics approval number [1]
3077
0
2006.173
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Summary
Brief summary
Randomised trial of two supraglottic airway devices by measuring objective outcomes in spontaneously breathing adult patients. Our hypothesis is that there will be no identifiable difference (null hypothesis).
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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
27608
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Address
27608
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Country
27608
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Phone
27608
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Fax
27608
0
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Email
27608
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Contact person for public queries
Name
10570
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Dr. Karl Alexander
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Address
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Department of Anaesthesia and Pain Management
The Royal Melbourne Hospital
Grattan Street
Parkville VIC 3050
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Country
10570
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Australia
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Phone
10570
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+61 3 93427540
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Fax
10570
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Email
10570
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[email protected]
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Contact person for scientific queries
Name
1498
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Dr David Andrews
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Address
1498
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Department of Anaesthesia and Pain Management
The Royal Melbourne Hospital
Grattan Street
Parkville VIC 3050
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Country
1498
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Australia
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Phone
1498
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+61 3 93427540
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Fax
1498
0
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Email
1498
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
No additional documents have been identified.
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