normal eyes
Conditions
Interventions
control group:30 eyes of randomly selected one of two eyes Vehicle solution was dropped 3 times a day during 2 day. In the second day, at 9, travoprost was dropped once.
treated group: contralateral
Sponsors
Department of Ophthalmology, University of Tokyo Faculty of Medicine
Miyata Eye Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: ophthalmologically normal eyes no systemic diseases
Exclusion criteria
Exclusion criteria: 1.treated or treating ocular or systemic disease 2.past history of ocular surgery 3.allergy for NSAIDs or PG-related drugs 4.wearing contact lenses during the study 5.using glaucoma drugs 6.using steroid drugs topically or systemically
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| intraocular pressure reduction hyperemia | — |
Countries
Japan
Contacts
Public ContactMakoto Aihara
University of Tokyo Faculty of Medicine Department of Ophthalology
Outcome results
None listed