Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07555574

Defining Retinal Structures Using Hyperspectral Retinal Imaging for Retinal and Optic Nerve Disease

Led by Center for Eye Research Australia · Updated on 2026-04-29

1000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating hyperspectral retinal imaging as a new, non-invasive method to capture detailed images of the retina and optic nerve in both healthy people and those with eye diseases. This study aims to compare hyperspectral imaging with standard eye imaging techniques to identify retinal biomarkers linked to diseases like diabetic retinopathy, glaucoma, and age-related macular degeneration. Around 1000 participants will take part in this research at ophthalmology clinics in Melbourne, Australia. Participants will undergo hyperspectral retinal imaging using specialized devices, including the Optina Diagnostics Metabolic Hyperspectral Retinal Camera and a prototype camera developed by the Centre for Eye Research Australia. This imaging captures the retina across multiple wavelengths to provide detailed spectral information beyond conventional photography. Alongside hyperspectral imaging, standard eye imaging tests such as OCT, OCT angiography, fundus photography, and autofluorescence will be performed for comparison. The study is observational and focuses solely on imaging analysis. During the study visit, participants will receive a full ophthalmic assessment including hyperspectral imaging and other standard imaging tests after pupil dilation. The collected images will be processed and analyzed using statistical and machine learning methods to extract detailed spectral data for each retinal pixel. Researchers will evaluate how well hyperspectral imaging can detect retinal diseases by comparing its data with established imaging biomarkers. The study will monitor the diagnostic performance of hyperspectral imaging throughout the data collection and analysis phases, with no therapeutic treatment involved.

CONDITIONS

Brief Title

Defining Retinal Structures Using Hyperspectral Retinal Imaging

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years and older
  • Able to provide informed consent
  • Willing and able to attend a study visit at the Centre for Eye Research Australia
  • Participants with diagnosed retinal or optic nerve disease (e.g., diabetic retinopathy, glaucoma, age-related macular degeneration)
  • Age- and sex-matched healthy control participants without known retinal or optic nerve disease
Not Eligible

You will not qualify if you...

  • Inability to provide informed consent
  • Ocular conditions preventing adequate retinal imaging (e.g., dense cataract, severe corneal opacity, vitreous haemorrhage)
  • Known contraindication to pharmacological pupil dilation
  • History of narrow anterior chamber angle or risk of angle closure glaucoma where dilation is considered unsafe
  • Any condition that, in the investigator's opinion, would compromise participant safety or image quality

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo non-invasive hyperspectral retinal imaging and standard ophthalmic assessments to characterize retinal and optic nerve structures.

1 visit (in-person)

Long-term Monitoring

Duration - Up to study completion

Hyperspectral images and clinical imaging data are analyzed to evaluate retinal disease detection, with no further active procedures for participants.

No additional visits required

Trial Site Locations

Total: 1 location

1

The Centre for Eye Research Australia

Melbourne, Victoria, Australia, 3002

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Research Team

D

Darvy Dang

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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Frequently Asked Questions

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