NCT00346593CompletedNot Applicable
Investigation of the Clinical Performance of Silicone Hydrogel Contact Lenses During Continuous Wear
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- University of Melbourne
- Locations
- 1
Study Overview
Brief Summary
The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens during continuous wear (up to 30 nights) over a period of 24 months.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- Double
Eligibility Criteria
- Ages
- 18 Years to 45 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Has had an oculo-visual examination in the last 2 years.
- •Is correctable to at least 6/7.5 distance visual acuity in each eye with spherical contact lenses.
- •Is a current 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.
Investigators
Study Sites (1)
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