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Trial registered on ANZCTR
Registration number
ACTRN12605000174684
Ethics application status
Approved
Date submitted
15/08/2005
Date registered
19/08/2005
Date last updated
19/08/2005
Type of registration
Prospectively registered
Titles & IDs
Public title
Anti-inflammatory effects of pioglitazone in acute stroke - a double-blind placebo controlled trial
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Scientific title
Anti-inflammatory effects of pioglitazone in acute stroke - a double-blind placebo controlled trial
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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 stroke
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Condition category
Condition code
Stroke
304
304
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0
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Ischaemic
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Pioglitazone 45mg/d given within 6 hours of ischaemic stroke and continued for 7 days.
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Comparator / control treatment
Placebo
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Control group
Placebo
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Outcomes
Primary outcome [1]
357
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Effect on various inflammatory markers
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Assessment method [1]
357
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Timepoint [1]
357
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At days 1, 3, 5, 7 and 14 after stroke.
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Secondary outcome [1]
805
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Stroke size and disability
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Assessment method [1]
805
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Timepoint [1]
805
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At 14 days.
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Eligibility
Key inclusion criteria
Diabetes, acute ischaemic stroke.
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Minimum age
Not stated
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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
Contra-indication to pioglitazone, unable to obtain consent, pregnant, severe inflammatory illness.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Numbered containers made up by hospital pharmacy.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Sequence generation will be via ClinStat (v3.2) software and will be stratified by patient sex.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/01/2007
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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
45
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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]
360
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Other
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Name [1]
360
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Address [1]
360
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Country [1]
360
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Primary sponsor type
Individual
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Name
Dr R W Simpson
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Address
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Country
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Secondary sponsor category [1]
286
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None
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Name [1]
286
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nil
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Address [1]
286
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Country [1]
286
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Ethics approval
Ethics application status
Approved
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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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Address
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Country
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Phone
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Fax
35668
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Email
35668
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Contact person for public queries
Name
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richard simpson
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Address
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Box Hill Hospital
Nelson Road
Box Hill VIC 3128
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Country
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Australia
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Phone
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+61 3 98953333
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
312
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Richard Simpson
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Address
312
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Box Hill Hospital
Nelson Road
Box Hill VIC 3128
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Country
312
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Australia
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Phone
312
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+61 3 98953333
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Fax
312
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Email
312
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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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