Eye scan to detect Alzheimer’s related protein deposits in adults with memory issues
Official title: Exploratory Study to Assess Utility of RetiSpec Artificial Intelligence Powered Retinal Imaging Solution in Detecting Amyloid Pathology in United Arab Emirates Nationals With Mild Impairment of Cognition
Run by Eli Lilly and Company · NCT07254234 · Data updated 2026-11-12
A screening eye test is being tried in adults with memory problems to see if retinal changes can signal Alzheimer’s-related protein deposits.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 55 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Eli Lilly and Company Industry-sponsored |
| Locations | 3 sites (Abu Dhabi and 2 other locations) |
| Status | Recruiting |
| Started | September 23, 2026 |
| Main results expected | September 2027 |
| Study ends | September 2027 |
| Registry record updated | September 24, 2026 |
| Trial ID | NCT07254234 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with mild memory complaints or mild cognitive impairment, who have APOE genotyping results available and a MoCA score between 22 and 28.
✕Probably not a fit
Individuals without detectable retinal changes linked to Alzheimer’s disease or who do not meet the inclusion criteria may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study screens adults with memory complaints or mild cognitive impairment to see if retinal imaging, alongside a blood test, can reveal changes linked to Alzheimer’s disease. Participants will undergo a retinal scan and a blood test during a single visit, with the total participation lasting up to one month. The study requires prior APOE genotyping results to be available to investigators and uses MoCA scores to describe cognitive status. The research is conducted at multiple Abu Dhabi sites led by Eli Lilly and Company, with no active intervention beyond diagnostic imaging and blood testing.
Why it matters
Potential benefit: If successful, the screening tools could help identify individuals at risk for Alzheimer’s-related changes earlier or more conveniently.
How similar studies have gone: Prior studies have explored retinal changes and biomarkers in Alzheimer’s, but this exact combined screening approach is being evaluated for feasibility.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants who are overtly healthy as determined by medical evaluation, including medical history and physical examination. * Have mild memory complaints or a diagnosis of mild cognitive impairment. * Have undergone genotyping for apolipoprotein E (APOE) and are willing to make results available to the investigator. * Montreal Cognitive Assessment (MoCA) score of greater than or equal to 22 and less than or equal to 28. Exclusion Criteria: * Have any medical condition that, in the opinion of the investigator, would be a contraindication to participation in the study. * Have an existing diagnosis of AD or other dementia. * Have contradictions to or an allergy to the ophthalmic dilating agents. * Have known diagnosis of severe glaucoma or severe cataracts; have a significant refractive error (more than 12 diopters \[D\] of spherical equivalent refraction); or have any ocular media opacity that prevents imaging of the retina (that is, severe cataract). Note: mild to moderate cataracts or vision correction with glasses or contact lenses are not exclusion criteria. * Current or previous treatment with anti-amyloid medications. * Are currently enrolled in any other clinical study involving an investigational product or any other type of medical research judged not to be scientifically or medically compatible with this study.
Where it's running
-
Sheikh Shakhbout Medical City
Abu Dhabi, United Arab Emirates Recruiting -
Sheikh Tahnoon Bin Mohammed Medical City
Abu Dhabi, United Arab Emirates Recruiting -
Burjeel Medical City
Abu Dhabi, United Arab Emirates Not yet recruiting
Study contacts
- Study coordinator: Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
- Email: LillyTrials@Lilly.com
- Phone: 1-317-615-4559
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.