Clinical evaluation of two types of daily disposable silicone hydrogel contact lenses in habitual CL wearers.

Mimura Tatsuya0 个研究点目标入组 50 人开始时间: 2021年9月24日最近更新: 2023年10月17日

适应症

试验速览

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•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

•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

发起方

Mimura Tatsuya