Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12613000801718
Ethics application status
Approved
Date submitted
17/07/2013
Date registered
19/07/2013
Date last updated
5/08/2013
Type of registration
Prospectively registered

Titles & IDs
Public title
Correlation between alcohol concentration and an electroencephalogram (EEG) measure of anaesthetic depth
Scientific title
The correlation between increasing breath alcohol concentration and Bispectral Index in anaesthetic registrars
Secondary ID [1] 282837 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
The impact of increasing alcohol on BIS (a measure of EEG activity used as a surrogate for anaesthetic depth) 289644 0
Condition category
Condition code
Anaesthesiology 289963 289963 0 0
Other anaesthesiology

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Participants will attend just one study day (for one four hour session). They will be asked to refrain from consuming caffeine from 10am on the study day. Only participants who are not rostered for clinical duties over the ensuing 24 hours will be able to participate in the study. Alcohol will be provided for study participants to consume over 3 hours. They will be asked to drink a similar amount of alcohol to that which they would normally drink at home or when out. The type and amount of alcohol consumed throughout the study will be recorded. Wine, beer, nonalcoholic drinks and snacks will be provided during the study period, and a meal will be provided at the end of the study. Four measurments of breath alcohol, and of BIS, will be taken for each participant (hourly, over the four hour study period) plus one set of baseline measurements. A single blood sample will be taken at the end of the study to confirm blood alcohol levels.
Intervention code [1] 287529 0
Other interventions
Comparator / control treatment
There is no comparator or control treatment for this study - as we are assessing the relationship between breath alcohol levels and BIS all participants will drink alcohol over the study period.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 290015 0
Correlation between end-expired (breathalyser) alcohol concentration and BIS.
Timepoint [1] 290015 0
Baseline (before drinking) and then every hour over four hours
Secondary outcome [1] 303777 0
Correlation between blood alcohol concentration and BIS.
Timepoint [1] 303777 0
Four hours after starting drinking (at study end)
Secondary outcome [2] 303778 0
Agreement and correlation between Anaesthetic Trainees’ predicted blood alcohol concentration and measured blood alcohol concentration
Timepoint [2] 303778 0
At each breath alcohol concentration reading (1, 2, 3 and 4 hours)

Eligibility
Key inclusion criteria
Anaesthetic Trainees (age between 25 and 40 years) who have completed their clinical duties on a Friday afternoon and are not rostered to work for at least 24 hours.
Minimum age
25 Years
Maximum age
40 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
History of epilepsy; currently taking any sedating medication including analgesics such as codeine and opioids, benzodiazepines, anti-epileptics and sleeping medications; history of liver disease or impaired liver function; currently pregnant.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
No allocation of treatment or concealment of treatment in this study.

Potential participants will be notified of the upcoming study at a department inservice. Potential participants (ie those not rostered on for working during the weekend following the study date) will be approached by a study coordinator.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
NA
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Pharmacokinetics / pharmacodynamics
Statistical methods / analysis
Correlation between blood alcohol concentration and BIS will be determined. This will be followed by multivariate regression analysis including various participant characteristics to further delineate the relationship between blood alcohol concentration and BIS. Sample size calculation for this kind of study is unreliable. A previous study on healthy patients showed mean baseline BIS scores to be in the mid 90s with minimal variation.[1] We plan to study 10-20 patients. With the benefit of repeated measurements, a sample size of 10 subjects measured on 4 occasions should provide power of greater than 80% (with an alpha value set at 0.05 and beta value of 0.2) to detect a correlation of 0.3 which would be clinically relevant.

1. Cortinez, L.I., et al., Performance of the cerebral state index during increasing levels of propofol anesthesia: a comparison with the bispectral index. Anesth Analg, 2007. 104(3): p. 605-10

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
25/07/2013
Actual
2/08/2013
Date of last participant enrolment
Anticipated
1/08/2013
Actual
2/08/2013
Date of last data collection
Anticipated
Actual
Sample size
Target
20
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 1316 0
The Alfred - Prahran
Recruitment outside Australia
Country [1] 5195 0
New Zealand
State/province [1] 5195 0
Auckland

Funding & Sponsors
Funding source category [1] 287619 0
University
Name [1] 287619 0
University of Auckland
Country [1] 287619 0
New Zealand
Primary sponsor type
University
Name
University of Auckland
Address
Department of Anaesthesiology
University of Auckland
Private Bag 92019
Auckland
New Zealand
1023
Country
New Zealand
Secondary sponsor category [1] 286365 0
Hospital
Name [1] 286365 0
The Alfred
Address [1] 286365 0
55 Commercial Rd, Melbourne VIC 3004, Australia
Country [1] 286365 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 289591 0
Health and Disability Ethics Committee
Ethics committee address [1] 289591 0
Ethics committee country [1] 289591 0
New Zealand
Date submitted for ethics approval [1] 289591 0
16/05/2013
Approval date [1] 289591 0
16/07/2013
Ethics approval number [1] 289591 0
13/NTA/90
Ethics committee name [2] 289592 0
Alfred Hospital Ethics Committee
Ethics committee address [2] 289592 0
Ethics committee country [2] 289592 0
Australia
Date submitted for ethics approval [2] 289592 0
18/03/2013
Approval date [2] 289592 0
17/06/2013
Ethics approval number [2] 289592 0
183/13

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 41466 0
A/Prof Simon Mitchell
Address 41466 0
Department of Anaesthesiology
University of Auckland
Private Bag 92019
Auckland
New Zealand
1023
Country 41466 0
New Zealand
Phone 41466 0
+64 9 3737599 ext 89300
Fax 41466 0
Email 41466 0
[email protected]
Contact person for public queries
Name 41467 0
Jacqueline Hannam
Address 41467 0
Department of Anaesthesiology
University of Auckland
Private Bag 92019
Auckland
New Zealand
1023
Country 41467 0
New Zealand
Phone 41467 0
+64 9 3737599 ext 89308
Fax 41467 0
Email 41467 0
[email protected]
Contact person for scientific queries
Name 41468 0
Jacqueline Hannam
Address 41468 0
Department of Anaesthesiology
University of Auckland
Private Bag 92019
Auckland
New Zealand
1023
Country 41468 0
New Zealand
Phone 41468 0
+64 9 3737599 ext 89308
Fax 41468 0
Email 41468 0
[email protected]

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
SourceTitleYear of PublicationDOI
EmbaseAcute alcohol intoxication and bispectral index monitoring.2015https://dx.doi.org/10.1111/aas.12546
N.B. These documents automatically identified may not have been verified by the study sponsor.