Nidek RS3000 Comparative Study
NCT01384487 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 89
Last updated 2012-02-20
Summary
The primary objective of this clinical study is to compare the Nidek RS-3000 Optical Coherence Tomography (OCT) device to the Optovue RTVue OCT. The secondary objective is to evaluate any adverse events found during the clinical study.
Conditions
- Glaucoma
- Retinal Disease
- Corneal Disease
Sponsors & Collaborators
-
Nidek Co. LTD.
lead INDUSTRY
Principal Investigators
-
Robert Weinreb, M.D. · UCSD, Hamilton Glaucoma Center
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-06-30
- Primary Completion
- 2011-11-30
- Completion
- 2011-11-30
Countries
- United States
Study Locations
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