None listed
Conditions
Interventions
None listed
Sponsors
Huvitz
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Male and female Western adults aged 22 years or older and under 85 years. Individuals who are able to comply with the instructions of the study investigator Individuals who have provided a written informed consent form to participate in the study Individuals with normal eyes
Exclusion criteria
Exclusion criteria: Koreans and other Asian ethnicities Individuals with physical or mental conditions that may interfere with study participation or compliance with study requirements Individuals with corneal injury or a history of corneal surgery, including corneal laser procedures Individuals who have worn hard contact lenses within the past 2 weeks, or soft contact lenses within 2 hours before examination Individuals with dry eye syndrome severe enough to potentially affect intraocular pressure Individuals with other conditions that may affect intraocular pressure Individuals with hypersensitivity to topical anesthetics or fluorescent dyes Individuals deemed by the investigator to be inappropriate for participation, or that may interfere with or confound the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intraocular pressure | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety | — |
Countries
Korea, Republic of
Contacts
Public ContactSunpil Shin
Dankook Univeristy Hospital
Outcome results
None listed