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Trial registered on ANZCTR
Registration number
ACTRN12605000592640
Ethics application status
Approved
Date submitted
12/09/2005
Date registered
5/10/2005
Date last updated
27/02/2008
Type of registration
Prospectively registered
Titles & IDs
Public title
The VALID study: is ventilation affected by leaving in dentures?
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Scientific title
To investigate whether bag-mask ventilation after induction of anaesthesia in patients with dentures is easier with dentures left in or removed.
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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:
Absent dentition
719
0
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Condition category
Condition code
Anaesthesiology
796
796
0
0
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Other anaesthesiology
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The patients randomised to Group A have their dentures removed after induction of anaesthesia but before bag-mask ventilation, while the patients randomised to Group B have their dentures left in for bag-mask ventilation and removed afterwards, prior to placement of endotracheal tube or laryngeal mask airway. Bag-mask ventilation is attempted in both groups of patients for 30 seconds after loss of eyelash reflex.
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Intervention code [1]
535
0
None
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
1017
0
Ease of bag-mask ventilation as determined by chest rise and fall
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Assessment method [1]
1017
0
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Timepoint [1]
1017
0
Measured for 30 seconds immediately after loss of eyelash reflex.
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Primary outcome [2]
1018
0
Ease of bag-mask ventilation as determined by presence of etCO2 trace at 3 litres/min fresh gas flow
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Assessment method [2]
1018
0
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Timepoint [2]
1018
0
Measured for 30 seconds immediately after loss of eyelash reflex.
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Primary outcome [3]
1019
0
Ease of bag-mask ventilation as determined by APL valve at 20cmH2O
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Assessment method [3]
1019
0
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Timepoint [3]
1019
0
Measured for 30 seconds immediately after loss of eyelash reflex.
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Secondary outcome [1]
1907
0
Fresh gas flow required in litres/min.
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Assessment method [1]
1907
0
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Timepoint [1]
1907
0
Assessed for 30 seconds immediately after loss of eyelash reflex.
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Secondary outcome [2]
1908
0
APL valve setting in cmH2O.
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Assessment method [2]
1908
0
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Timepoint [2]
1908
0
Assessed for 30 seconds immediately after loss of eyelash reflex.
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Secondary outcome [3]
1909
0
Requirement to use oxygen flush valve.
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Assessment method [3]
1909
0
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Timepoint [3]
1909
0
Assessed for 30 seconds immediately after loss of eyelash reflex.
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Secondary outcome [4]
1910
0
Requirement for oropharyngeal airway.
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Assessment method [4]
1910
0
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Timepoint [4]
1910
0
Assessed for 30 seconds immediately after loss of eyelash reflex.
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Secondary outcome [5]
1911
0
Requirement for second person to assist to seal the mask.
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Assessment method [5]
1911
0
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Timepoint [5]
1911
0
Assessed for 30 seconds immediately after loss of eyelash reflex.
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Eligibility
Key inclusion criteria
All patients with dentures undergoing general anaesthesia excluding those unable to give informed consent and those having rapid sequence induction were invited to participate
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Minimum age
No limit
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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
No exclusion criteria
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Study design
Purpose of the study
Diagnosis
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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)
sequence concealed in numbered envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated block randomisation with random block size
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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
10/10/2005
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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
162
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
208
0
New Zealand
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State/province [1]
208
0
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Funding & Sponsors
Funding source category [1]
885
0
Self funded/Unfunded
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Name [1]
885
0
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Address [1]
885
0
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Country [1]
885
0
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Primary sponsor type
Hospital
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Name
Dunedin Public Hospital
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Address
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Country
New Zealand
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Secondary sponsor category [1]
747
0
None
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Name [1]
747
0
N/A
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Address [1]
747
0
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Country [1]
747
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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
36404
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Address
36404
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Country
36404
0
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Phone
36404
0
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Fax
36404
0
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Email
36404
0
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Contact person for public queries
Name
9724
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Dr. Matthew Zacharias
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Address
9724
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Department of Anaesthesia
Dunedin Public Hospital
201 Great King St
Dunedin
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Country
9724
0
New Zealand
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Phone
9724
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+64 3 4740999 ext. 8030
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Fax
9724
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+64 3 4747650
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Email
9724
0
[email protected]
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Contact person for scientific queries
Name
652
0
Dr. Niamh Conlon
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Address
652
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Dept of Anesthesiology, PO Box 3094, Duke University Medical Center, Durham, NC 27710.
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Country
652
0
United States of America
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Phone
652
0
001 919 6811965
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Fax
652
0
001 919 6818993
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Email
652
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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