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Trial registered on ANZCTR
Registration number
ACTRN12605000220662
Ethics application status
Approved
Date submitted
11/08/2005
Date registered
26/08/2005
Date last updated
18/11/2019
Date data sharing statement initially provided
18/11/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Ketamine by intravenous, sublingual and oral route of administration for treatment of pain:pharmacokinetics
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Scientific title
Ketmine by intravenous, sublingual and oral route of administration for treatment of pain: pharmacokinetics
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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:
Acute pain
303
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Condition category
Condition code
Alternative and Complementary Medicine
346
346
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0
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Pain management
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Adminstration of oral, sublingual, intravenous ketamine for patints in acute pain.
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Intervention code [1]
168
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None
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Comparator / control treatment
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
401
0
Drug pharmacokinetics for 8 hours after oral and sublingual routes of administration compared with intravenous
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Assessment method [1]
401
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Timepoint [1]
401
0
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Secondary outcome [1]
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Nil
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Assessment method [1]
873
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Timepoint [1]
873
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Eligibility
Key inclusion criteria
Previously on ketamine.
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Minimum age
18
Years
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Maximum age
Not stated
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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
Coronary artery disease,hypertension,tachyarrythmias,impaired renal function,pregnancy,lactation.
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
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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
10/05/2005
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Actual
1/06/2005
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Date of last participant enrolment
Anticipated
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Actual
1/10/2005
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Date of last data collection
Anticipated
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Actual
5/10/2005
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Sample size
Target
10
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Accrual to date
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Final
6
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
406
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Other Collaborative groups
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Name [1]
406
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ANZCA grant 2004
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Address [1]
406
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Country [1]
406
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Primary sponsor type
Individual
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Name
Professor Stephan Schug
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Address
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Country
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Secondary sponsor category [1]
329
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Hospital
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Name [1]
329
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Royal Perth Hospital
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Address [1]
329
0
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Country [1]
329
0
Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1390
0
Royal Perth Hospital
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Ethics committee address [1]
1390
0
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Ethics committee country [1]
1390
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Australia
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Date submitted for ethics approval [1]
1390
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10/07/2004
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Approval date [1]
1390
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23/09/2004
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Ethics approval number [1]
1390
0
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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
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Prof Stepahn Schug
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Address
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UWA Anaesthesia
L2 MRF Bld. Royal Perth Hospital
Box X2213 Perth 6847
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Country
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Australia
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Phone
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+61 0412299025
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Fax
36290
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Email
36290
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[email protected]
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Contact person for public queries
Name
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Stephan Schug
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Address
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University of Western Australia
2nd Floor
Medical Research Foundation Building
GPO Box X2213
Perth WA 6847
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Country
9357
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Australia
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Phone
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+61 8 92240201
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Fax
9357
0
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Email
9357
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[email protected]
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Contact person for scientific queries
Name
285
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Stephan Schug
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Address
285
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Department Anaesthesia & Pain Medicine
Royal Perth Hospital
Welington Street
Perth WA 6000
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Country
285
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Australia
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Phone
285
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+61 8 92241036
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Fax
285
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+61 8 92241111
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Email
285
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
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No/undecided IPD sharing reason/comment
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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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