OCT Agreement and Precision Study
NCT02045823 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 66
Last updated 2022-06-08
Summary
To demonstrate clinical substantial equivalence of 3D OCT-1 Maestro as comparable to the commercially available iVue and NW-300. Also, to demonstrate clinical substantial equivalence of 3D OCT-2000 Maestro as comparable to the commercially available NW-300.
Conditions
- Normal Eyes
- Eyes With Glaucoma
- Eyes With Retinal Disease
Sponsors & Collaborators
-
Topcon Medical Systems, Inc.
lead INDUSTRY
Principal Investigators
-
Mike Sinai, PhD · Topcon Corporation
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-01-31
- Primary Completion
- 2014-03-31
- Completion
- 2014-03-31
Countries
- United States
Study Locations
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