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Clinical Trials/JPRN-UMIN000010975
JPRN-UMIN000010975
Not yet recruiting
未知

Effects of 3% diquafosol sodium ophthalmic solution on visual function in patient with dry eye wearing contact lens. - Effects of 3% diquafosol sodium ophthalmic solution on visual function in patient with dry eye wearing contact lens.

Minamiaoyama Eye Clinic Tokyo0 sites20 target enrollmentJune 30, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Minamiaoyama Eye Clinic Tokyo
Enrollment
20
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 30, 2013
End Date
December 31, 2013
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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