Clinical Trials in the USA / NCT07796230
Recruiting
Observational
Modified P200TE Data Collection
NCT07796230 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Retina Disease
Investigational drug(s) / intervention(s)
imaging device
imaging device: images captured on a modified P200TE
Study summary
Images will be collected on the modified P200TE
Eligibility
Inclusion Criteria
Male or female participants 22 years of age or older who have full legal capacity to volunteer on the date the informed consent is signed
Participants who can follow the instructions by the clinical staff at the clinical site
Participants who agree to participate in the study
Participants with posterior segment eye disease. Example of pathologies may include but are not limited to Age-related macular degeneration, glaucoma, diabetic retinopathy, posterior uveitis, central serous chorioretinopathy, vein occlusion, epiretinal membrane and others as confirmed by the investigator.
Exclusion Criteria
Participants unable to tolerate ophthalmic imaging.
Participants with ocular media not sufficiently clear to obtain acceptable images.
Unable to obtain acceptable image quality on participant.
Primary outcome measure(s)
- Number of images — 1 year
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Bennett & Bloom Eye Centers | Louisville | Kentucky | 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 NCT07796230 on ClinicalTrials.gov ↗ ← All trials in the USA