Comparative Study of Specular Microscope for Cell Density, Coefficient of Variation, Hexagonality and Corneal Thickness
NCT01729975 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80
Last updated 2012-11-21
Summary
The primary objective of this clinical study is to collect clinical data to support an FDA 510(k) submission for the Nidek Specular Microscope CEM-530. The secondary objective is to evaluate any adverse events found during the clinical study.
Conditions
- Corneal and Endothelial Cell Measurements
Sponsors & Collaborators
-
Nidek Co. LTD.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-10-31
- Primary Completion
- 2012-10-31
Countries
- United States
Study Locations
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