Triton Reference Database
Completed
- Conditions
- Healthy Eyes
- Interventions
- Device: Topcon DRI OCT Triton (plus)
- Registration Number
- NCT03067675
- Lead Sponsor
- Topcon Corporation
- Brief Summary
The objective of this study is to collect OCT measurement data on normal healthy eyes.
- Detailed Description
The objective of this study is to collect OCT measurement data on normal healthy eyes in order to determine the reference limits for Topcon DRI OCT Triton based on the percentile points for 1%, 5%, 95%, and 99%.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Subjects Presenting With Normal Eyes Topcon DRI OCT Triton (plus) Subjects with no known ocular diseases will be scanned on the Topcon DRI OCT Triton (plus) device
- Primary Outcome Measures
Name Time Method Retinal Thickness 1 Minute The thickness of the macula layer
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (6)
Southern California College of Optometry
🇺🇸Anaheim, California, United States
Accessoreyes Optometry
🇺🇸Pasadena, California, United States
Illinois College of Optometry
🇺🇸Chicago, Illinois, United States
Stat University of New York College of Optometry
🇺🇸New York, New York, United States
New York VA
🇺🇸Jamaica, New York, United States
Fischer Laser Eye Center
🇺🇸Willmar, Minnesota, United States