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Tests a new handheld retinal scanner in adults and children with eye disease

Tests a new self-aligning handheld eye scanner in adults and children with eye conditions.

Plain-language title generated from the registry record
Registry title: Advancing Pediatric Retinal Imaging With Auto-aligned OCT

Key facts

Where
Durham, United StatesSee the site

Where in United States

  • Duke University Eye CenterDurham, United StatesTaking people

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Trial details

Who runs it
Duke University
Trial code
NCT06841575
Record updated
25 March 2026
Original description
The goal of the current study is to conduct a pilot study to test a new version of the handheld OCT device capable of auto-alignment to image the retina in adult volunteers, and adult and pediatric patients in clinic.Read full original descriptionShow less

Advancing Pediatric Retinal Imaging With Auto-aligned OCT

The goal of the current study is to conduct a pilot study to test a new version of the handheld OCT device capable of auto-alignment to image the retina in adult volunteers, and adult and pediatric patients in clinic.

Inclusion: Group 1: Healthy adult volunteers; Subject is able and willing to consent to study participation; Subject is more than 18 years of age; Healthy adult volunteers without known ocular issues other than refractive error; Group 2: Adult patients in ophthalmology clinics; Health care provider, knowledgeable of protocol, agrees that study personnel could contact the subject; Subject is able and willing to consent to study participation; Subject is more than 18 years of age and is a patient in the Duke Eye Center ophthalmology clinics; Group 3: Pediatric participants in ophthalmology clinics; Health care provider, knowledgeable of protocol, agrees that study personnel could contact the parent/legal guardian; Parent/legal guardian is able and willing to consent to study participation; Pediatric patient less than 18 years of age in Duke Eye Center ophthalmology clinics or undergoing clinically-indicated examination under anesthesia at Duke Eye Center.

Exclusion: Subjects with prior problems with pupil dilation; Pregnant woman if receiving dilating drops; Participant has a health or eye condition that preclude eye examination or retinal imaging (such as corneal opacity or cataract); Participant has a health or eye condition that preclude eye examination or retinal imaging (such as corneal opacity or cataract); Group 1: Healthy adult volunteers; Students or employees under direct supervision of the investigators; Group 2: Adult patients in ophthalmology clinics; Group 3: Pediatric participants in ophthalmology clinics; Parent/legal guardian unwilling or unable to provide consent.

ClinicalTrials.gov NCT06841575