NCT06250868CompletedNot Applicable
TRK-3 Agreement and Precision of Pachymetry Function
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Topcon Corporation
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Cornea thickness
Study Overview
Brief Summary
To evaluate the performance of a new tonometer.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 22 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Provide voluntary written consent for participation in the study.
- •Age at least 22 years old at the time of informed consent.
Exclusion Criteria
- •Ocular condition that may affect the ability to perform corneal measurement (e.g., corneal perforation, bullous keratopathy, nystagmus)
- •Have or is suspected to have an ocular infection in either eye.
- •Otherwise considered unsuitable for the study by the investigator
- •Unable to tolerate ophthalmic testing.
Outcomes
Primary Outcomes
Cornea thickness
Time Frame: 1 day
Thickness of the cornea
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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