Widefield Confocal Scanning Laser Ophthalmoscope Optimized for Pediatric and Neonatal Imaging
Recruiting now
Conditions studied: Eye Diseases
In brief
The goal of this observational study is to test the use of a novel Widefield Confocal Scanning Laser Ophthalmoscope (WiSLO) Optimized for Pediatric and Neonatal Imaging in pediatric and adult subjects who are undergoing clinical evaluation for eye disease or are healthy adult volunteers. The main questions to answer are: * Whether WiSLO will be more comfortable and satisfactory in experience for the patient and operator than commercial alternatives. * If the quality of WiSLO near infrared images will be comparable to color fundus camera imaging across population of different ages and fundus pigmentation. Participants will have the following research procedures: * Imaging of both eyes with a research noncontact WiSLO * Imaging of both eyes with a commercially available non-contact hand held fundus camera (Volk Pictor Plus) * Likert scales for adults * Pediatric Likert scales for children * CRIES scales for infants.
Key facts
- Study ID
- NCT06177639
- Run by
- Duke University
- People needed
- 42
- Starts
- 2025-10-01
- Expected to finish
- 2026-08-01
- Last updated by the study team
- 2025-10-08
Who can join
Age: 0 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adults (≥18 years) that may or may not have eye pathology
- Infant/child undergoing clinically-indicated examination that may or may not have eye pathology. NOTE: We will not enroll inpatient pre-term infants or neonates. The youngest age at enrollment will be 30 days adjusted age using the NICH NRN Web-based Adjusted Age Calculator.
- Adults and infant/child with or without prior pupil dilation for clinical eye care visit
- Adult participant is able and willing to consent to study participation
- Parent/Legal Guardian is able and willing to consent to study participation for the minor
- Pediatric participant >12 years is able and willing to assent to study participation
You may not qualify if…
- Participant or Parent/Legal Guardian unwilling or unable to provide consent
- Participant has a health or eye condition that would preclude eye examination or retinal imaging (e.g. evidence of inflammation or infection of ocular surface or eyelids, or corneal opacity or cataract)
Where it is running
- Duke University Eye Center — Durham, North Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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