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Clinical Trials in Australia / NCT07545473
Recruiting Not applicable

Retinal Hyperspectral Imaging in Neurodegenerative Diseases

NCT07545473 · tracked via the Priya Life Science Australia tracker
Phase
Not applicable
Started
2021-10-11
Last updated
2026-04-22

Condition(s) studied

DementiaNeurodegenerative DiseasesAlzheimer DiseaseParkinson DiseaseFrontotemporal DementiaVascular DementiaLewy Body DiseaseNiemann-Pick Diseases

Investigational drug(s) / intervention(s)

Hyperspectral camera

Hyperspectral camera: Hyperspectral imaging is performed with the Metabolic Hyperspectral Retinal Camera (Optina Diagnostic, Montreal, Canada) and a prototype camera developed by researchers at the Centre for Eye Research Australia (CERA). The Metabolic Hyperspectral Retinal Camera is similar to a typical fundus imager but it incorporates a tunable light source which is able to transmit safe light levels within a wavelength range covering the visible to near infrared with a narrow bandwidth (\< 3nm). This instrument is capable of imaging a 26° field-of-view of retina at 90 wavelengths in less than a second, thus minimizing discomfort and limiting the influence of eye movements. The hyperspectral camera developed by CERA researchers is a non-mydriatic fundus camera that uses light emitting diodes (LEDs) and an optical variable bandpass filter to tune the illumination wavelengths.

Study summary

Hyperspectral retinal imaging is a non-invasive imaging modality in which a series of images of the retina are captured using light of different wavelengths. The resulting "hypercube" of data provides a wealth of information about the retinal structure. Our group has developed evidence supporting a role for this technology in the detection of retinal amyloid beta in Alzheimer's disease. We are undertaking further studies to establish the role of this method in the assessment of people with dementia, or those at risk of Alzheimer's disease. In addition, we wish to test whether the approach may have value in other forms of dementia or neurodegenerative disease such as Parkinson's disease, Lewy-Body dementia or vascular dementia.

Eligibility

Sex
ALL
Min age
30 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1. Aged over 30 years. 2. Have dementia or a neurodegenerative disease such as Alzheimer's disease, Parkinson's disease, Lewy body dementia, Niemann-Pick type 2 or vascular dementia (age-matched and sex-matched controls will also be recruited). 3. With the exception of participants with Parkinson's disease and Lewy body disease, for whom clinical examination by a neurologist is sufficient to establish a clinical diagnosis of probable dementia with Lewy Body or probable Parkinson disease dementia, all participants must have previously undergone at least of one of the following tests to help to confirm a clinical diagnosis of dementia or neurodegenerative disease: genetic tests, blood biomarker tests (amyloid, tau, neurofilament light), a brain amyloid beta PET scan, or cerebrospinal fluid tests. 4. Have a minimum best corrected visual acuity level of 6/60 in both eyes and no major eye problems, such as advanced age-related macular degeneration, advanced glaucoma, or greater than moderate non-proliferative diabetic retinopathy. 5. Be willing to participate in the study and attend the Centre for Eye Research Australia. 6. Be accompanied by a friend or family member. Exclusion Criteria: 1. Inability to provide informed consent 2. Ocular conditions preventing adequate retinal imaging (e.g., dense cataract, severe corneal opacity, vitreous haemorrhage) 3. Known contraindication to pharmacological pupil dilation 4. Any condition that, in the investigator's opinion, would compromise participant safety or image quality

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Centre for Eye Research Australia Melbourne Victoria Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07545473 on ClinicalTrials.gov ↗ ← All trials in Australia