normal controls and patients with ocular hypertention
Conditions
Interventions
Measuring ocular pressure
Sponsors
Nagoya University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: People who were able to be measured the ocularpressure
Exclusion criteria
Exclusion criteria: The pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of ocular pressure measured by MR-600 and usual tonometer | — |
Countries
Japan
Contacts
Public ContactUeno Shinji
Nagoya university hospital ophthalmology
Outcome results
None listed