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Cheap eye scanner could bring retinal checks to the masses
NCT ID NCT05530460
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a custom, low-cost eye imaging device to see if it can produce retinal images as good as those from expensive commercial machines. Eleven healthy adults had their retinas scanned with both devices. The goal was to check if the cheaper device could clearly show the retina's structure, which could help make eye screening more affordable worldwide.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- low-cost optical coherence tomography device
- What this could lead to
- If successful, this could make retinal imaging more affordable and accessible, especially in low-resource settings.
- What could go wrong
- This is a very small, early-stage device comparison with only 11 participants. It does not test treatment or health outcomes, only image quality.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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11 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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May 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * able to provide informed consent Exclusion Criteria: * potentially confounding ocular conditions, such as: glaucoma, current corneal injury, retinal damage, diabetes, corrected distance visual acuity worse than 20/40 * eyes that have had intraocular surgery, other than cataract surgery If two eyes satisfy the inclusion / exclusion criteria, both eyes will be included in the study. If only one eye satisfies the criteria, only the qualifying eye will be included in the study.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Duke University Medical Center
Durham, North Carolina, 27710, United States
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