Agreement and Precision Study
Completed
- Conditions
- Eye AbnormalitiesNormal Eyes
- Registration Number
- NCT06733428
- Lead Sponsor
- Topcon Corporation
- Brief Summary
To evaluate the performance of pachymetry function
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 108
Inclusion Criteria
- Provide voluntary written consent
- Age at least 22 years old
- For glaucoma group only, visual field defect and optic nerve damage consistent with glaucoma
- For cornea group only, cornea abnormality
Exclusion Criteria
- Ocular condition that may affect ability to perform cornea measurements
- Have or is suspected to have ocular infection
- Unable to tolerate eye testing
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cornea thickness 1 day thickness of the cornea
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
How does TRK-3 pachymetry compare to OCT and ultrasound in measuring corneal thickness precision?
What biomarkers correlate with TRK-3 pachymetry accuracy in keratoconus and Fuchs' dystrophy?
What are the technical limitations of TRK-3 versus Pentacam and IOLMaster in corneal thickness assessment?
How does Topcon's TRK-3 pachymetry perform in eyes with post-refractive surgery abnormalities?
What are the clinical implications of TRK-3 precision for glaucoma management and IOP measurement?
Trial Locations
- Locations (1)
Illinois College of Optometry
🇺🇸Chicago, Illinois, United States