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Modified P200TE Data Collection
RecruitingObservational studyHealthy volunteers welcome
Who can join
Ages 22 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
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.
About the study
Images will be collected on the modified P200TE
What is being tested
- imaging device (device)
Sponsor: Optos, PLC · Participants: 50 · Started: Jul 29, 2026
Contact the study team
Official record on ClinicalTrials.gov — NCT07796230
Locations in the U.S.
| Kentucky | Bennett & Bloom Eye Centers, Louisville |
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.