NCT02447120CompletedNot Applicable
Topcon 3D OCT-1 Maestro Reference Database Study II
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Topcon Medical Systems, Inc.
- Enrollment
- 504
- Locations
- 7
- Primary Endpoint
- Retinal Thickness
Study Overview
Brief Summary
The objective of this study is to collect OCT measurement data on normal healthy eyes in order to determine the reference limits for Topcon 3D OCT-1 Maestro based on the percentile points for 1%, 5%, 95%, and 99%.
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 3D OCT-1 Maestro based on the percentile points for 1%, 5%, 95%, and 99%.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Retinal Thickness
Time Frame: 1 minute
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (7)
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