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Trial registered on ANZCTR
Registration number
ACTRN12605000098639
Ethics application status
Approved
Date submitted
5/08/2005
Date registered
8/08/2005
Date last updated
8/08/2005
Type of registration
Prospectively registered
Titles & IDs
Public title
Predictive value and reaction times of skin conductivity versus bispectral index for assessment of awakening after balanced anaesthesia
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Scientific title
Predictive value and reaction times of skin conductivity versus bispectral index for assessment of awakening after balanced anaesthesia
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Universal Trial Number (UTN)
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Trial acronym
SCA BAL
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
bispectral index/skin conductance
179
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Condition category
Condition code
Skin
202
202
0
0
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Normal skin development and function
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Anaesthesiology
203
203
0
0
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Other anaesthesiology
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Intraoperative monitoring of bispectral index/skin conductance.
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Intervention code [1]
127
0
None
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
242
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Reaction times of bispectral index vs. skin conductance regarding postoperative awaking
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Assessment method [1]
242
0
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Timepoint [1]
242
0
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Secondary outcome [1]
549
0
Correlation of bispectral index.
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Assessment method [1]
549
0
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Timepoint [1]
549
0
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Secondary outcome [2]
550
0
Skin conductance with clinical signs of awareness.
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Assessment method [2]
550
0
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Timepoint [2]
550
0
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Eligibility
Key inclusion criteria
Patients ASA physical status 1-3, body weight within normal limits (+/- 15 % of normal body weight (height minus 100 in kg)).
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Minimum age
18
Years
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Maximum age
65
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
Known dependency on alcohol or nicotine; epileptic; peripheral vascular disease or autonomic neuropathy potentially involving the hand; on medication known to interfere with normal responses to the sympathetic nervous system (e.g. beta-blockers, atropine); pacemaker.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/09/2005
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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
25
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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]
257
0
Commercial sector/Industry
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Name [1]
257
0
MED Storm Innovations
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Address [1]
257
0
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Country [1]
257
0
Norway
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Primary sponsor type
Hospital
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Name
Departmental funding Dept. of Anaesthesia Royal Perth Hospital
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Address
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Country
Australia
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Secondary sponsor category [1]
196
0
None
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Name [1]
196
0
n/a
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Address [1]
196
0
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Country [1]
196
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1085
0
Royal Perth Hospital
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Ethics committee address [1]
1085
0
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Ethics committee country [1]
1085
0
Australia
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Date submitted for ethics approval [1]
1085
0
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Approval date [1]
1085
0
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Ethics approval number [1]
1085
0
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Summary
Brief summary
Two monitoring devices (Skin conductance and bispectral index) are tested regarding their predictive value and reaction times for postoperative awaking.
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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
35414
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Address
35414
0
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Country
35414
0
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Phone
35414
0
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Fax
35414
0
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Email
35414
0
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Contact person for public queries
Name
9316
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Thomas Ledowski
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Address
9316
0
Department of Anaesthesia and Pain Medicine
Royal Perth Hospital
Wellington Street
Perth WA 6000
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Country
9316
0
Australia
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Phone
9316
0
+61 8 92242797
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Fax
9316
0
+61 8 92241111
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Email
9316
0
[email protected]
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Contact person for scientific queries
Name
244
0
Thomas Ledowski
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Address
244
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Department of Anaesthesia and Pain Medicine
Royal Perth Hospital
Wellington Street
Perth WA 6000
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Country
244
0
Australia
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Phone
244
0
+61 8 92242797
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Fax
244
0
+61 8 92241111
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Email
244
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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