Evaluation of the changes of quantity and quality of tears by instillation of lipid-containing commercial eye drops.
Phase 4
- Conditions
- Dry eye
- Registration Number
- JPRN-UMIN000005340
- Lead Sponsor
- Department of Ophthalmology, Kyoto Prefectural University of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
Anyone who is considered to be inappropriate for this study (ex. Any allergic history to Systane Balance, Dry Aid® EX and SoftSantear®, women who are under pregnant or lactation period)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tear film breakup time, corneal and conjunctival epithelial damage score, tear meniscus radius, Schirmer test(I), spreading velocity of tear film lipid layer
- Secondary Outcome Measures
Name Time Method