Effects of 3% diquafosol sodium ophthalmic solution on visual function in patient with dry eye wearing contact lens.
Not Applicable
- Conditions
- dry eye
- Registration Number
- JPRN-UMIN000010975
- Lead Sponsor
- Minamiaoyama Eye Clinic Tokyo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1) History of administered diquafosol sodium ophthalmic solution and/or rebamipide ophthalmic solution within one week before start of study. 2) Anatomically and/or functionally abnormal eyelid. (ex. eyelid closure abnormality) 3) History of ophthalmic surgery (including laser therapy) within 3 months before start of study. 4) History of occluding punctum. (ex. punctal plug or a punctal closing surgery) 5) Presence of a hypersensitivity to drugs scheduled to be used. (ex. diquafosol sodium, fluorescein, oxybuprocaine hydrochloride) 6) Presence of any other medical concern that may affect the accurate efficacy assessment or ensuring safety.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method