The curative effect of Diquafosol Sodium ophthalmic solution 3% to the diabetic who has the amount fall of tear fluid secretion, and an anterior-epithelium-of-cornea obstacle.
- Conditions
- diabetes with an anterior-epithelium-of-cornea obstacle
- Registration Number
- JPRN-UMIN000010912
- Lead Sponsor
- Tokyo Women's Medical University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 45
Not provided
1.The user of a contact lens (used within one week or the existing patient who is going to use a contact lens during medical treatment observation) 2.The patient who has the past of cornea refractive surgery. 3.The patient currently diagnosed as meibomian gland dysfunction. 4.The patient suffered from eye infection or a serious allergic conjunctival disease. 5.The patient currently diagnosed as the cicatricial angle conjunctival disease (eye pemphigoid, and Stevens-Johnson syndrome and alkali externally caused injury are included). 6.The patient who has the past of an inner eye operation (laser surgery is included) within three months before an observation start. 7.The patient who was continuing the medical treatment (a punctum plug insertion way, a surgical punctum closing way, etc.) aiming at the blockade of punctum before the observation term start till less than one month. 8.The patient who is performing dry eye auxiliary medical treatment which has on pharmacometrics, such as glasses for dry eye protection. 9.The patient who has eyeblink insufficiency. 10.The patient who has a schedule which adds an applying- ophthalmic solution during exam. 11.The patient with the schedule which uses the medicine (treatment) provided in the regulation about a concomitant drug (treatment) during exam. 12.The patient who had complications of the heart, liver, the kidney, blood dyscrasia, and others, and was judged to be unsuitable on pharmacometrics. 13.The patient who there is under pregnancy and breast-feeding or a possibility of having become pregnant, or wishes to become pregnant within one month after the scheduled end of an observation period.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method