Myopia
Conditions
Brief summary
The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens over a period of 6 months of extended wear.
Interventions
Sponsors
Menicon Co., Ltd.
Clinical Vision Research Australia
University of Melbourne
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Inclusion criteria
* Is correctable to at least 6/9 distance visual acuity in each eye with spherical contact lenses. * Is a current daily wear soft contact lens wearer. * Has no clinically significant anterior eye findings. * Has no other active ocular disease.
Exclusion criteria
* Has any systemic disease that might interfere with contact lens wear * Is using any systemic or topical medications that will affect ocular health. * Has any pre-existing ocular irritation that would preclude contact lens fitting. * Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses. * Has undergone corneal refractive surgery. * Is pregnant, lactating or planning a pregnancy.
Countries
Australia
Outcome results
None listed