Clinical effects of 3% diquafosol ophthalmic solution in dry eye disease patients using VDT
Not Applicable
- Conditions
- Dry Eye
- Registration Number
- JPRN-UMIN000008990
- Lead Sponsor
- Tokyo Electric Power hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients who had allergic conjunctivitis, uveitis or diabetic keratopathy 2)Patients who are satisfied with the current treatment for dry eye 3)Patients determined as ineligible for the study by the attending physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in subjective symptoms
- Secondary Outcome Measures
Name Time Method Changes in fluorescein staining scores and BUT