determination for the effect of reducing the daily variation of intraocular pressure for glaucoma patients, before and after the addition of Ripasudil 0.4% eye drops using the trigger fish system
Not Applicable
Recruiting
- Conditions
- glaucoma
- Registration Number
- JPRN-UMIN000041093
- Lead Sponsor
- Yokohama City University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients already on Ripasudil 0.4% eye drops 2) Patients who cannot wear contact lenses (patients with contraindicated target diseases as listed in the Triggerfish package insert) 3) Patients who cannot continue to use Ripasudil 0.4% due to hypersensitivity or other problems to eye drops 4) Other patients who are deemed unsuitable for inclusion in the subject by the physician's judgment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method