Examination of the effect of topical Rebamipide after the vitreous surgery in dry eye patients
Phase 4
- Conditions
- Dry eye patients underwent vitreous surgery
- Registration Number
- JPRN-UMIN000010457
- Lead Sponsor
- agasaki University Graduate School of Biomedical Sciences, Department of Ophtalmology
- Brief Summary
There was no statistical difference in corneal fluorescein score, subjective symptom score, and tear fluid break up time between the rebamipide group and the control group after vitrectomy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
Ocular surface disease other than dry eye Pregnant or lactating patient Rebamipide allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fluorescein corneo-conjunctival staining score
- Secondary Outcome Measures
Name Time Method Photophobia, Misty vision, Asthenopia, Feeling of dryness, Foreign-body sensation, Eye pain