New eye scanner software could sharpen diagnosis of macular degeneration
NCT ID NCT02827071
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested a new software called AngioScan, used with an already-approved eye camera, to see if it can take better pictures of the back of the eye. Researchers looked at 150 patients with retinal problems like macular degeneration. The goal was to find out if the software helps doctors see and diagnose eye diseases more clearly.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AngioScan angiography software (used with an FDA-approved OCT camera)
- What this could lead to
- If successful, this software could help doctors get clearer images of the eye, potentially leading to better diagnosis and treatment of retinal diseases.
- What could go wrong
- The software is not yet FDA-approved, and the study was terminated early, so results may be limited. It is a small, early-stage imaging study, not a treatment trial.
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.
- Participants
-
150 people
The number who actually took part.
- Start date
-
Jul 2016
- Finished
-
Dec 2021
- Lead sponsor
-
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.
Who is studied
Subjects with retinal vascular abnormalities
- Ages
-
18 to 115 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: • Any patient with abnormal retinal findings as determined by investigators. Exclusion Criteria: * Those suffering from head, neck or other injury which makes them unable to position themselves in head restraint for imaging. * Participants who are unable to maintain retinal fixation on a specified target. * Participants unable to achieve sufficient pupil dilation and alignment stability for imaging to take place. * Patients with media opacity which preclude high quality imaging.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Stein Eye Institute/Geffen School of Medicine
Los Angeles, California, 90095, United States
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Other studies related to the condition(s) this trial covers.
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