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Trial registered on ANZCTR
Registration number
ACTRN12612000797875
Ethics application status
Approved
Date submitted
24/08/2011
Date registered
30/07/2012
Date last updated
30/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Peak plasma propofol levels during endoscopy
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Scientific title
Peak plasma propofol levels in endoscopy patients receiving a Propofol-only anaesthetic
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Secondary ID [1]
262910
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Nil
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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:
Peak level of propofol in plasma during endoscopy with propofol only anaesthesia
270636
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Condition category
Condition code
Anaesthesiology
270807
270807
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0
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Anaesthetics
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Patients will receive propofol-only anaesthesia using the intermittent bolus technique.
Propofol will be administered through an intravenous cannula using the intermittent bolus technique (large loading bolus followed by small frequent boluses) which titrates dosage to adequate sedation.
The anaesthetist looking after the patient will give a propofol-only anaesthetic as per his or her usual procedure. The timing and dosage of boluses will not be stipulated by the researchers.
The loading dose is given immediately prior to commencing the endoscopy. Further boluses are given when deemed required by the anaesthetist.
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Intervention code [1]
269259
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Treatment: Drugs
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Comparator / control treatment
Nil
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Plasma propofol levels
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Assessment method [1]
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Timepoint [1]
279500
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2, 5 and 10 minutes
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Secondary outcome [1]
287761
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Nil
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Assessment method [1]
287761
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Timepoint [1]
287761
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Nil
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Eligibility
Key inclusion criteria
Undergoing colonoscopy or gastroscopy
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Minimum age
18
Years
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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
ASA 3 or 4
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
NA
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
NA
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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
Single group
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Other design features
Nil
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Phase
Phase 4
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Type of endpoint/s
Pharmacokinetics
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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
8/09/2011
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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
10
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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]
269726
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Hospital
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Name [1]
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Monash Medical Centre
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Address [1]
269726
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Department of Anaesthesia and Perioperative Medicine
Monash Medical Centre
246 Clayton Rd
Clayton
VIC 3168
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Country [1]
269726
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Australia
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Primary sponsor type
Hospital
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Name
Monash Medical Centre
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Address
Department of Anaesthesia and Perioperative Medicine
Monash Medical Centre
246 Clayton Rd
Clayton
VIC 3168
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
284522
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Address [1]
284522
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Country [1]
284522
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
271694
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Southern Health HREC
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Ethics committee address [1]
271694
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246 Clayton Rd Clayton VIC 3168
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Ethics committee country [1]
271694
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Australia
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Date submitted for ethics approval [1]
271694
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24/08/2011
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Approval date [1]
271694
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Ethics approval number [1]
271694
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Summary
Brief summary
The peak plasma propofol levels of endoscopy patients (Derived mathematically from the 3 measurements) along with the context sensitive half time of propofol (determined by the length of infusion) will allow the researchers to determine the time taken for plasma propofol levels to drop below levels known to cause driving impairment and thus estimate how long it takes for patients to drive safely after receiving a propofol only anaesthetic.
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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
33069
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Address
33069
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Country
33069
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Phone
33069
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Fax
33069
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Email
33069
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Contact person for public queries
Name
16316
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Sud Agarwal
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Address
16316
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Department of Anaesthesia and Perioperative Medicine
Monash Medical Centre
246 Clayton Rd
Clayton
VIC 3168
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Country
16316
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Australia
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Phone
16316
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+61395956666
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Fax
16316
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Email
16316
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[email protected]
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Contact person for scientific queries
Name
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Sud Agarwal
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Address
7244
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Department of Anaesthesia and Perioperative Medicine
Monash Medical Centre
246 Clayton Rd
Clayton
VIC 3168
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Country
7244
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Australia
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Phone
7244
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+61395956666
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Fax
7244
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Email
7244
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[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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