glaucoma
Conditions
Interventions
The study subjects used the research instruments tap-eye tonometer and the control instruments GAT and NCT. The observation period is one month, and two examinations are carried out baseline and one m
Sponsors
Teshigawara Tsuyoshi
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Cases that the principal investigator has determined that the test can be conducted. Prior to entry into this study, consent must be made by signing the explanatory consent form. The following conditions are the eligibility criteria Normal eye and glaucoma eye Glaucoma study subjects do not need to interrupt routine eye drop treatment. Age:18 years old or older Gender:no restrictions
Exclusion criteria
Exclusion criteria: Research subjects who fall under one or more of the following items will be excluded from this study: (a) Less than one month after eye surgery (b) When there is a possibility that an ophthalmologist consultation is required during the clinical research period (c) In addition, when the Principal Investigator judges that the Principal Investigator is inappropriate as the subject of this research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation coefficient with other tonometer (coefficient of determination: R2) The correlation coefficient when compared with this instrument and the recognized ocular pressure gauge (GAT, NCT) is evaluated. At that time, the evaluation index showed a statistically significant correlation following the previously published paper | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Coincidence rate of change in intraocular pressure over time 2) Reproducibility in the same study subjects | — |
Contacts
Public ContactAkira Kitamura
Yokohama Tsurumi Chuo Eye Clinic
Outcome results
None listed