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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

Sponsor: Optos, PLC · Participants: 50 · Started: Jul 29, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07796230

Locations in the U.S.

KentuckyBennett & 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.