Image Evaluation of Intalight Dream OCTA Scans With Optos FA & ICGA Images
Intalight, Inc
30 participants
Mar 25, 2026
OBSERVATIONAL
Conditions
Summary
The goal of this study is to evaluate the image quality and clinical utility of the OCTA images from the VG200D OCT device (investigational device) compared against the FA and ICGA images from the UWF Optos California (CA) device. Image assessment will be conducted by three expert image graders and involve the assessment of the images based on both image quality and clinical utility. Evidence for substantial equivalence will be obtained through establishing similar image evaluation results across the devices based on image quality and clinical utility.
Eligibility
Inclusion Criteria4
- Subjects 22 years of age or older on the date of informed consent
- Subjects able to understand the written informed consent and willing to participate as evidenced by signing the informed consent
- BCVA 20/400 or better in the study eye
- Diagnosis of retinal associated pathology by investigator with the need to have an FA and/or ICGA performed in at least one eye
Exclusion Criteria3
- Subjects unable to tolerate ophthalmic imaging
- Subjects not able to obtain acceptable OCT images due to ocular media opacity or other reasons
- Subject has a condition or is in a situation which the investigator feels may put the subject at significant risk, may confound the study results, or may interfere significantly with the subject's participation in the study
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
This study employs the Dream OCT to image the eyes of patients with retina pathology
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07568704