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Modified P200TE Data Collection

Optos, PLC · NCT07796230

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 22+ · All sexes
Healthy volunteers
Accepted
Study type
Observational
Target enrollment
50
US sites recruiting
1
Study start
July 29, 2026
Record last updated
September 1, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

Images will be collected on the modified P200TE

Being studied: imaging device

Conditions: Retina Disease

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full 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.

Recruiting US locations

  • Bennett & Bloom Eye Centers

    Louisville, KY 40222

    Site contact: Megan Kingdon · (502) 895-0040 · megankingdon@eyecarepartners.com

All healthy volunteers studies in Kentucky →
Modified P200TE Data Collection (NCT07796230) | Bored Studies