A randomized study comparing topical rebamipide with artificial tears in the treatment of dry eye with contact lens wearers
Not Applicable
- Conditions
- dry eye
- Registration Number
- JPRN-UMIN000011397
- Lead Sponsor
- Department of Ophthalmology, Keio University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
People with anterior segment eye diseases except dry eye disease Patients with severe posterior segment eye diseases Patients who use steroid, anti-inflammatory and immune suppression drugs Patients who take any anti-oxidant supplements. Patients with serious systemic diseases Patients who had any ocular surgery within 12 month prior to signing the informed consent Patients who had any punctual occlusion within 1 month prior to signing the informed consent People whom the investigator or the subinvestigators consider to be ineligible for the intervention therapy in any other reason
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method dry eye parameters (subjective and objective findings)
- Secondary Outcome Measures
Name Time Method