Healthy volunteers
Conditions
Interventions
Eyebon mild
Saline solution
Sponsors
Kobayashi Pharmaceutical Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Healthy subjects whose age of 20 years or more and 60 years or less 2.Subjects of soft contact lens user 3.Subjects who scored 11 or higher on the J-CLDEQ-8 questionnaire 4.Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study and being able to personally sign a written informed consent
Exclusion criteria
Exclusion criteria: 1.Subjects diagnosed with ocular Xerophthalmia(dry eye syndrome) 2.Subjects who have experienced adverse reactions such as skin rash, redness, itching, redness of the skin, redness of the eyes, itching or swelling of the eyes due to the use of eye washes in the past 3.Subjects with severe eye pain 4.Subjects who used eye washes or eye drops outside the study during the study period 5.Subjects infected with HBV, HCV, HIV, etc 6.Subjects who the investigator considers ineligible for enrolment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1: Evaluation of J-CLDEQ-8 scores | — |
Secondary
| Measure | Time frame |
|---|---|
| 2: Evaluation of conjunctival vascular occupancy 3: Evaluation of noninvasive interferometry break up time 4: Evaluation of mucin content in tear fluid 5: Evaluation of tear fluid volume 6: Determination of the amount of total protein adhered to contact lenses | — |
Countries
Japan
Contacts
Public ContactKengo Ito
Kobayashi Pharmaceutical Co., Ltd. R&D Healthcare Division
Outcome results
None listed