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Trial registered on ANZCTR
Registration number
ACTRN12625000013460
Ethics application status
Approved
Date submitted
29/11/2024
Date registered
9/01/2025
Date last updated
3/06/2025
Date data sharing statement initially provided
9/01/2025
Type of registration
Prospectively registered
Titles & IDs
Public title
Optical coherence tomography imaging of the back of the eyes of healthy participants to develop automated measurement software
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Scientific title
Swept source optical coherence tomography angiography imaging of the posterior eye of participants with healthy eyes to develop automated segmentation software
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Secondary ID [1]
313496
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Nil known
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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:
Myopia is the health condition which will ultimately be the focus of the outcomes of this study.
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Condition category
Condition code
Eye
332509
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0
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Normal eye development and function
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Intervention/exposure
Study type
Observational
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Patient registry
False
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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
The choroid and layers of the posterior eye will be imaged using the Triton swept source OCT angiography instrument in participants with healthy eyes to allow development of automated segmentation software. The software delineates the thickness of individual tissue layers in the eye. The software can be later used in the development of myopia interventions to slow eye growth.
The images provide a cross section of the eye tissues.
The scanning protocols to be used include:
• Horizontal line scans (9 mm width) – 6 times
• Five-line cross scan (6 mm width) – 6 times
• Radial scan pattern (6 mm width) – 6 times
• Angiography scans – 3D Macula (3 mm volumetric) – 6 times
A typical scanning protocol involves:
• Adjusting the participant’s head/eye position in the Triton headrest until they can see the Triton’s internal fixation target
• Instructing the participant to continue watching the fixation target during the scans and the likely length of the scan time
• Instructing the participant to blink twice and then waiting 2-3 seconds before the scan commences to ensure a high-quality tear distribution and optimal scan quality
• Instructing the participant to sit back from the instrument and relax before commencing the next set of scans
The scanning protocol typically requires a few minutes per scan and there are four different scanning protocols.
There will be a single visit with total duration of about 60 minutes.
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Intervention code [1]
330071
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The perfusion (blood flow) of the choroid will be measured.
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Assessment method [1]
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Angiography scans will provide an estimate of blood flow/perfusion in the blood vessels of the choroid. Blood perfusion is based on an arbitrary scale from zero (no blood perfusion) to 1 (active perfusion) in a defined region of tissue and is derived from changes in "speckle" (or graininess) in successive OCT images.
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Timepoint [1]
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Scans of the posterior eye will be conducted at one 60 minute visit.
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Primary outcome [2]
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The primary outcome of the image analysis will include the thickness of the choroid between the boundaries of the retinal pigment epithelium (RPE) and chorio-scleral interface (CSI).
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Assessment method [2]
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Segmentation provides the thickness of the various eye tissues including the choroid and retina. The segmentation will be based on the OCT imaging B scans including the horizontal and radial line scans. The tissue thickness is derived in microns, limited by the pixel size of the OCT image.
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Timepoint [2]
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Scans of the posterior eye will be conducted at one 60 minute visit.
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Secondary outcome [1]
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Nil
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Assessment method [1]
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Nil
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Timepoint [1]
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Nil
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Eligibility
Key inclusion criteria
Good vision
Healthy eyes
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Minimum age
18
Years
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
The presence of cataracts will interfere with the optical coherence tomography scans and participants with cataracts will be excluded.
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Convenience sample
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Timing
Prospective
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Statistical methods / analysis
The development of deep learning (artificial intelligence) software for segmenting optical coherence tomography images requires a set of reference images for "training" the software. We will acquire reference images from 40 participants. Based on previous work in our laboratory and numerous other published papers in this field, a dataset of at least 20 reference images is sufficient to allow the development of accurate segmentation software (ie. better than 99% accuracy in tissue layer detection).
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
17/01/2025
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Actual
22/01/2025
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Date of last participant enrolment
Anticipated
11/04/2025
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Actual
12/04/2025
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Date of last data collection
Anticipated
30/04/2025
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Actual
12/04/2025
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Sample size
Target
40
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Accrual to date
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Final
40
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Recruitment in Australia
Recruitment state(s)
QLD
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Johnson and Johnson Vision Care
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Address [1]
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Country [1]
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United States of America
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Primary sponsor type
University
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Name
Queensland University of Technology
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Address
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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]
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Address [1]
320282
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Country [1]
320282
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Queensland University of Technology University Human Research Ethics Committee
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Ethics committee address [1]
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https://www.qut.edu.au/research/why-qut/ethics-and-integrity
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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05/03/2024
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Approval date [1]
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11/03/2024
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Ethics approval number [1]
316617
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8211
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Summary
Brief summary
Swept source optical coherence tomographers (SS-OCTs) provide high resolution images of the eye and have an enhanced depth of focus (greater scanning depth in tissue) compared to conventional (spectral domain) OCTs. These additional features allow for blood flow characteristics in the retina and choroid to be quantified (OCT Angiography) without the use of any additional dyes, drugs or contact with the eye. This is a prospective data collection study which aims to capture clinical data of the choroid with the Triton swept source OCT including angiography. In order to enhance the vascular characteristics analysis, software tools will later be developed by the project team.
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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 Michael Collins
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Address
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Optometry and Vision Science, QUT, O Block, Victoria Park Rd, Kelvin Grove, 4059, QLD
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Country
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Australia
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Phone
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+61 413 246913
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Michael Collins
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Address
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Optometry and Vision Science, QUT, O Block, Victoria Park Rd, Kelvin Grove, 4059, QLD
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Country
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Australia
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Phone
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+61 413 246913
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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
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Michael Collins
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Address
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Optometry and Vision Science, QUT, O Block, Victoria Park Rd, Kelvin Grove, 4059, QLD
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Country
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Australia
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Phone
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+61 413 246913
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Fax
138436
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Email
138436
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[email protected]
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Data sharing statement
Will the study consider sharing individual participant data?
No
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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