myopic astigmatism myopic astigmatism
Conditions
Interventions
Randomly select the first SCL and use it for 2 weeks, then switch to the other SCL.
Sponsors
Mimura Tatsuya
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.The consent in writing has obtained. In the case of a minor patient, the consent of the representative in addition to the patient should be obtained 2.Aged 13 to 40 years old must sign the informed consent 3.Habitual soft silicone hydrogel contact lenses wearers 4.Requiring lenses within the power range of both study contact lenses to be fitted (-0.50D to -6.00D) 5.Vision correctable 0.8 (20/25) or better in each eye at distance with pre-study contact lenses at Baseline 6.daily disposable silicone hydrogel contact lenses in habitual CL wearers 7.Have subjective symptoms of dry eye as defined by the Symptomatology eligibility questionnaires
Exclusion criteria
Exclusion criteria: 1.Subjects with systemic disease 2.Use of systemic or local antibiotics or corticosteroids 3.Use of immunomodulatory 4.pregnancy or breastfeeding 5.History of eye surgery trauma within 6 months of the enrollment visit 6.Current wearing DT1 or 1-Day Acuvue TruEye sphere lenses 7.Subjects who have no appropriate judgement 8.Those who work for a company that manufactures and sells contact lenses 9.Patient who in judged ineligible as patients in this clinical study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total score of DEQ 5 (questionnaire regarding wearing). Two groups, the new SCL Precision One and the existing SCL One Day Acuvue True Eye, will be compared. | — |
Secondary
| Measure | Time frame |
|---|---|
| Total score of J-CLDEQ-8 (questionnaire on the comfort of wearing CL) Two groups, the new SCL Precision One and the existing SCL One Day Acuvue True Eye, will be compared. | — |
Contacts
Public ContactTatsuya Mimura
Teikyo University Hospital
Outcome results
None listed