Healthy volunteers
Conditions
Interventions
To investigate the ocular blood flow alterations in response to intraocular pressure elevation on two different days.
Sponsors
Tohoku University Graduate School of Medicine, Department of Ophthalmology
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy volunteers Normal findings in slit lamp and funduscopic examinations No history of ophthalmic or general disorders, prior ocular laser or incisional surgery in either eye, and the use of systemic or topical medication Obtain written-informed consent from the subjects.
Exclusion criteria
Exclusion criteria: A regular smoking habit High myopia Baseline intraocular pressure less than 22mmHg in both eyes History of topical medication allergy In pregnancy History of unconfortable for periocular compression History of ophthalmic or general disorders, prior ocular laser or incisional surgery in either eye, and the use of systemic or topical medication No written-informed consent from the subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Ocular blood flow ratio and coefficient of variation in the intraocular pressure elevation phase was calculated with reference to this baseline. | — |
Countries
Japan
Contacts
Public ContactYukihiro Shiga
Tohoku University Graduate School of Medicine Department of Ophthalmology
Outcome results
None listed