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Trial registered on ANZCTR
Registration number
ACTRN12612000344897
Ethics application status
Approved
Date submitted
19/03/2012
Date registered
26/03/2012
Date last updated
26/03/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Intravitreal Steroid for Anterior Ischemic Optic Nerve disease.
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Scientific title
The effect of intravitreal triamcinolone on best corrected visual acuity (BCVA) and visual field in patients with non-arteritic anterior ischemic optic neuropathy.
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Secondary ID [1]
280168
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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:
Non-arteritic Anterior Ischemic Optic Neuropathy
286098
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Condition category
Condition code
Eye
286291
286291
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0
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Diseases / disorders of the eye
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
An intravitreal injection of 4 mg/0.1ml triamcinolone acetonide
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Intervention code [1]
284497
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Treatment: Drugs
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Comparator / control treatment
observation with standard care
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Control group
Active
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Outcomes
Primary outcome [1]
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BCVA) according to the Snellen chart (converted to logMAR units) at twelfth week
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Assessment method [1]
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Timepoint [1]
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twelfth week
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Primary outcome [2]
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Mean deviation of automated perimetry 30-2 on a Humphrey field analyzer
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Assessment method [2]
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Timepoint [2]
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twelfth week
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Secondary outcome [1]
296603
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Retinal nerve fiber layer thickness using Optical Coherence Tomography (OCT)
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Assessment method [1]
296603
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Timepoint [1]
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twelfth week
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Eligibility
Key inclusion criteria
- acute painless visual loss
- localized optic disc edema
- no associated symptoms (; i.e. headache/scalp tenderness/jaw claudication)
- unilateral involvement with the normal fellow eye
- no previous attack or treatment
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Minimum age
50
Years
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Maximum age
75
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
- ocular and/or orbital infection
- other ocular disease that might interfere with visual acuity and/ or the visual field
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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)
- All of the patients were randomized into two groups: one treated with IVTA while the other was simply observed.
- allocation concealment by sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Permuted block randomization
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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 3
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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
1/04/2012
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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
20
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
4208
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Thailand
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State/province [1]
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Khon Kaen
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Khon Kaen University
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Address [1]
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Faculty of Medicine, Khon Kaen University, Mitraparp Road, Muang, Khon Kaen, Thailand 40002
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Country [1]
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Thailand
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Primary sponsor type
University
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Name
Khon Kaen University
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Address
Faculty of Medicine, Khon Kaen University, Mitraparp Road, Muang, Khon Kaen, Thailand 40002
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Country
Thailand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
283792
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Human Ethic Commitee of Khon Kaen University
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Ethics committee address [1]
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Faculty of Medicine, Khon Kaen University, Mitraparp Road, Muang, Khon Kaen, Thailand 40002
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Ethics committee country [1]
286917
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Thailand
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Date submitted for ethics approval [1]
286917
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Approval date [1]
286917
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Ethics approval number [1]
286917
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Summary
Brief summary
The purpose of this study was to determine the effect of intravitreal triamcinolone acetonide (IVTA), compared to careful observation, in restoration of optic nerve functions.
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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
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Email
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Contact person for public queries
Name
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Kitthisak Kitthaweesin
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Address
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Department of Ophthalmology
Faculty of Medicine, Khon Kaen University, Mitraparp Road, Muang, Khon Kaen, Thailand 40002
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Country
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Thailand
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Phone
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6643348383
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Fax
17188
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6643348383
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Email
17188
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[email protected]
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Contact person for scientific queries
Name
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Kitthisak Kitthaweesin
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Address
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Department of Ophthalmology
Faculty of Medicine
Khon Kaen University
Khon KaeFaculty of Medicine, Khon Kaen University, Mitraparp Road, Muang, Khon Kaen, Thailand 40002
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Country
8116
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Thailand
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Phone
8116
0
6643348383
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Fax
8116
0
6643348383
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Email
8116
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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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