Evaluation of efficacy of diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution on treatment of dry eye (multicenter study).
Not Applicable
- Conditions
- Dry eye
- Registration Number
- JPRN-UMIN000009071
- Lead Sponsor
- Ehime University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients who use artificial tears eyedrops within 2 weeks before a study starts. 2) Patients who need to use eyedrops other than test drugs during a study . 3) Patients who have anatomically and functionally abnormal eyelid. 4) Patients who develop allergic conjunctivitis disease requiring treatment when a study starts. 5) Patients who underwent ophthalmic surgery within 3 months before study starts ( however LASIK within 6 months). 6) Patient who have a previous history of treatment intended to become obstructed lacrimal puncta. 7) Patients who have a previous allergy to drugs that they use during a study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Symptoms and Tear film breakup time
- Secondary Outcome Measures
Name Time Method