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Trial registered on ANZCTR
Registration number
ACTRN12609001050246
Ethics application status
Approved
Date submitted
2/12/2009
Date registered
8/12/2009
Date last updated
10/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
The influence of surgery on sevoflurane brain levels and awakening after anaesthesia.
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Scientific title
To investigate the relationship between the invasiveness of surgery and the point at which patients awaken after anaesthesia and surgery.
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Secondary ID [1]
1178
0
Nil
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Universal Trial Number (UTN)
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Trial acronym
SW Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Anaesthetics
252220
0
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First-response time following surgery.
252360
0
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Gall bladder problems
252362
0
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Bowel conditions
252363
0
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Condition category
Condition code
Anaesthesiology
252239
252239
0
0
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Anaesthetics
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Surgery
256547
256547
0
0
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Surgical techniques
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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
major bowel surgery and "simple" laparoscopic surgery -determining time of first-response after surgery, pain scores in Post Anaesthetic Care Unit (PACU), time to reach PACU discharge criteria, recovery score. Observed, when possible, up to 48 or 76 hrs post-surgery.
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Intervention code [1]
241446
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Not applicable
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Comparator / control treatment
Two surgical groups:
1. Intermediate surgery ('simple laparoscopic surgery)
2. Major surgery - major bowel surgery/liver resections & surgery of similar 'invasiveness'
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Control group
Active
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Outcomes
Primary outcome [1]
253113
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Sevoflurane & fentanyl levels in blood and effect site.
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Assessment method [1]
253113
0
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Timepoint [1]
253113
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First response (time of patient response to 'open-eye' command) post operatively
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Secondary outcome [1]
257983
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Worst post-operative pain score in recovery as assessed on the standard 0-5 scale (where 0=no pain & 5=extreme pain) routinely used in PACU.
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Assessment method [1]
257983
0
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Timepoint [1]
257983
0
Prior to discharge from Recovery.
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Secondary outcome [2]
257989
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Quality of Recovery score .
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Assessment method [2]
257989
0
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Timepoint [2]
257989
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Prior to discharge from hospital.
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Eligibility
Key inclusion criteria
Non-emergency surgery
American Society of Anesthetists (ASA) 1, 2 or 3
Body Mass Index (BMI) less than 35
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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
Contra-indication to propofol.
Contra-indication to sevoflurane.
Contra-indication to fentanyl.
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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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
7/05/2009
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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
105
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
2272
0
New Zealand
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State/province [1]
2272
0
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Funding & Sponsors
Funding source category [1]
256120
0
Self funded/Unfunded
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Name [1]
256120
0
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Address [1]
256120
0
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Country [1]
256120
0
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Primary sponsor type
Hospital
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Name
Christchurch Hospital
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Address
Private Bage 4710
Rolleston Ave
Christchurch 8140
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Country
New Zealand
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Secondary sponsor category [1]
251464
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None
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Name [1]
251464
0
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Address [1]
251464
0
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Country [1]
251464
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
244032
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Upper South B Regional Ethics Committee
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Ethics committee address [1]
244032
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C/- Ministry of Health 4th floor 250 Oxford Terrace PO Box 3877 Christchurch 8140
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Ethics committee country [1]
244032
0
New Zealand
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Date submitted for ethics approval [1]
244032
0
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Approval date [1]
244032
0
06/05/2009
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Ethics approval number [1]
244032
0
URB/08/05/025
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Summary
Brief summary
Previous audit data has suggested the magnitude of surgery has an influence on calculated effect site sevoflurane levels at awakening. The aim of this study is to evaluate this difference using a structured anaesthetic technique so as to minimise confounding variables. As intrathecal morphine (ITM) has become a common adjunct in major surgery we are also exploring the effect of ITM on effect site sevoflurane
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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
30402
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Address
30402
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Country
30402
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Phone
30402
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Fax
30402
0
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Email
30402
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Contact person for public queries
Name
13649
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Margie McKellow
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Address
13649
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c/o Department of Anaesthesia
Christchurch Hospital
2 Riccarton Avenue
Private Bag 4710
Christchurch 8011
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Country
13649
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New Zealand
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Phone
13649
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+64 3 3640288
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Fax
13649
0
+64 3 3640289
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Email
13649
0
[email protected]
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Contact person for scientific queries
Name
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Assoc Prof Ross Kennedy
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Address
4577
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c/o Department of Anaesthesia
Christchurch Hospital
2 Riccarton Avenue
Private Bag 4710
Christchurch 8011
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Country
4577
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New Zealand
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Phone
4577
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+64 3 3640288
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Fax
4577
0
+64 3 3640289
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Email
4577
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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