Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
250 participants
OBSERVATIONAL
2025-03-04
2029-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Presence of pachyvessels on ultra-widefield (UWF) imaging in at least one quadrant.
3. Willing to undergo pupil dilation, and protocol-required procedures for both eyes
4. Willing to provide written informed consent
Exclusion Criteria
2. Eyes with other ocular pathology such as trauma, inflammation, previous intraocular surgery (except for cataract surgery)
3. Systemic diseases that might affect ocular blood flow such as uncontrolled hypertension, autoimmune disease, and haematological disorders
4. Pregnant or nursing women
5. Persons who are unable to give informed consent
45 Years
ALL
No
Sponsors
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National University Hospital, Singapore
OTHER
University of Malaya
OTHER
Hong Kong University
OTHER
Singapore National Eye Centre
OTHER_GOV
Responsible Party
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Gemmy Cheung Chui Ming
Professor
Locations
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Hong Kong University
Hong Kong, , Hong Kong
University of Malaya Medical Centre
Kuala Lumpur, , Malaysia
National University Hospital, Singapore
Singapore, , Singapore
Singapore National Eye Centre/ Singapore Eye Research Institute
Singapore, , Singapore
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-4359
Identifier Type: -
Identifier Source: org_study_id
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