Myopic astigmatism
Conditions
Interventions
Sponsors
Higuchi Hirohiko
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Aged 18 to 40 years old, and gender is not a factor. 2.Subjects who are able to understand an informed consent form. 3.Subjects to whom the study lens can be prescribed within the power range. 4.Subjects with a CL corrected visual acuity of 0.7 or higher to whom the lens is a good fit. 5.Subjects who wear CL on both eyes for at least 8 hours per day and 7 days per week. 6.Subjects who have no health conditions that would be a problem for the usage of CL.
Exclusion criteria
Exclusion criteria: 1.Subjects who wear a contact lens in only one eye. 2.Subjects with aphakia or eyes implanted with artificial intraocular lenses. 3.Subjects with systemic diseases that may affect the eyes. 4.Subjects using drugs that may affect visual function and CL performance. 5.Subjects with keratoconus, corneal infiltration, or corneal ulcer. 6.Subjects who have undergone ophthalmic surgery refractive surgery, etc. 7.Subjects who are participating in other clinical studies or clinical trials, or who have participated in studies or trials in the past 30 days. 8.Subjects who the researcher in charge of the clinical trial deems unsuitable.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Daily disposable silicone hydrogel contact lens comfort assessment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Daily disposable silicone hydrogel contact lens fitting assessment. | — |
Contacts
Public ContactKimiko Kato
ROHTO NITTEN Co., Ltd.
Outcome results
None listed