Myopia Clinical Trial
The primary purpose of this study is to investigate the performance of contact lens maintenance systems when used with silicone hydrogel contact lenses during daily wear over a period of 1 month.
Status | Completed |
Enrollment | 44 |
Est. completion date | December 2006 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Is correctable to at least 20/40 distance visual acuity in each eye with spherical contact lenses. - Is an experienced soft contact lens wearer for at least 1 month. - Has no clinically significant anterior eye findings. - Has no other active ocular disease. Exclusion Criteria: - Requires concurrent ocular medication. - Eye surgery or injury within 12 weeks prior to enrolment. - Has any systemic disease or ocular abnormality that might interfere with contact lens wear - Has any pre-existing ocular irritation that would preclude contact lens fitting. - PMMA lens wear previous 6 months. - EW or CW in previous 1 month. - Hydrogen peroxide users - Latex sensitivity |
Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Australia | Clinical Vision Research Australia | Carlton | Victoria |
Lead Sponsor | Collaborator |
---|---|
University of Melbourne | CIBA VISION |
Australia,
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