Inclusion criteria
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• The participants were (males or females) over 20 years old with open angle glaucoma or OHT, poorly controlled by ophthalmic solutions and requiring additional treatment |
• Prior treatment with one or more of prostaglandin (PG) analogs, and/or beta-blockers, and/or acetazolamide |
• No history of treatment with ripasudil ophthalmic solution |
Exclusion criteria
|
• Participants with hypersensitivity against ripasudil hydrochloride hydrate, anhydrous dihydrogen phosphate sodium, glycerin, sodium hydroxide, or concentrated benzalconium chloride liquid |
• Less than −12 dB of mean deviation (MD) value |
• Women of childbearing potential who were pregnant, nursing, or planning a pregnancy |
• Secondary glaucoma (excluding exfoliation glaucoma) |
• Angle closure glaucoma |
• Refract value: Less than −9.0 D, More than +9.0 D |
• Participants whose intra ocular pressure cannot be measured by the iCare Tonometer |
• Participants with traumatic injuries |
• Participants with ocular inflammation of the anterior segment |
• Participants who cannot tolerate photo slit |
• Participants having with histories of surgeries during the past 6 months. |
• Users of contact lenses |
• Individuals deemed unsuitable for this trial by doctors |