Comparative Study of Non-contact Tonometers for Intraocular Pressure and Corneal Cell Thickness Measurements
NCT02138279 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65
Last updated 2022-06-08
Summary
The primary objective of this clinical study is to collect clinical data to support FDA 510(k) submissions for the Topcon CT-800, CT-1, CT-1P and TRK-2P non-contact tonometers. The secondary objective is to evaluate any adverse events found during the clinical study.
Conditions
- Intraocular Pressure
- Corneal Pachymetry
Sponsors & Collaborators
-
Topcon Medical Systems, Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-04-30
- Primary Completion
- 2014-07-31
- Completion
- 2014-12-31
Countries
- United States
Study Locations
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