Actively Recruiting
Image Evaluation of Intalight Dream OCTA Scans With Optos FA & ICGA Images
Led by Intalight, Inc · Updated on 2026-05-06
30
Participants Needed
1
Research Sites
22 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Image Evaluation of Intalight Dream OCTA Scans With Optos FA & ICGA Images
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects 22 years of age or older on the date of informed consent
- Able to understand and willing to sign the informed consent
- Best corrected visual acuity (BCVA) of 20/400 or better in the study eye
- Diagnosed with retinal associated pathology requiring FA and/or ICGA in at least one eye
You will not qualify if you...
- Unable to tolerate ophthalmic imaging
- Unable to obtain acceptable OCT images due to ocular media opacity or other reasons
- Having a condition or situation that may put the subject at significant risk or interfere with study participation as judged by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Retina Consultants of Texas
Houston, Texas, United States, 77401
Actively Recruiting
Research Team
M
Mike Sinai, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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