A study of the intraocular pressure lowering effect of topical application of ripasudil in clinical practice
Not Applicable
- Conditions
- Glaucoma
- Registration Number
- JPRN-UMIN000025466
- Lead Sponsor
- Kobe University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 130
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who underwent laser suturelysis intoraocular surgery other than glaucoma surgery by 6 months after the initiation of ripasudil eyedrops.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Magnitude and percentage of IOP reduction 6 months after initiation of ripasudil application
- Secondary Outcome Measures
Name Time Method