Myopia Clinical Trial
Official title:
Evaluation of the Performance of Different Daily Disposable Lens Designs in Habitual Soft Contact Lens Wearers
Verified date | September 2021 |
Source | Coopervision, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main objective of the study is to refit existing soft lens wearers with two different daily disposable contact lens types, Lens A and Lens B, to determine their performance after one week of wear.
Status | Completed |
Enrollment | 68 |
Est. completion date | February 5, 2021 |
Est. primary completion date | February 5, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Is at least 18 years of age and has full legal capacity to volunteer; 2. Has read and signed an information consent letter; 3. Self reports having a full eye examination in the previous two years; 4. Anticipates being able to wear the study lenses for at least 8 hours a day, 7 days a week; 5. Is willing and able to follow instructions and maintain the appointment schedule; 6. Habitually wears soft contact lenses, for the past 3 months minimum; 7. Has refractive astigmatism no higher than -0.75DC in each eye; 8. Can be fit and achieve binocular distance vision of at least 20/30 Snellen (Available lens parameters are sphere -1.00 to -6.00D, 0.25D steps). Exclusion Criteria: 1. Is participating in any concurrent clinical or research study; 2. Habitually wears one of the study contact lenses; 3. Has any known active* ocular disease and/or infection that contraindicates contact lens wear; 4. Has a systemic condition that in the opinion of the investigator may affect a study outcome variable; 5. Is using any systemic or topical medications that in the opinion of the investigator may affect contact lens wear or a study outcome variable; 6. Has known sensitivity to the diagnostic sodium fluorescein used in the study; 7. Self-reports as pregnant, lactating or planning a pregnancy at the time of enrolment; 8. Has undergone refractive error surgery or intraocular surgery. |
Country | Name | City | State |
---|---|---|---|
United States | Athens Eye Care | Athens | Ohio |
United States | Nittany Eye Associates | College | Pennsylvania |
United States | Complete Eye Care of Medina | Medina | Minnesota |
United States | Sacco Eye Group, PLLC | Vestal | New York |
Lead Sponsor | Collaborator |
---|---|
Coopervision, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Lens Wettability | Lens wettability on a 0 to 4 descriptive scale, 0.5 steps (0 - Very poor: Immediately displaying non-wetting areas on the lens surface, immediate drying time, 1 - Poor: Irregular surface appearance, drying time << blink time, 2 - Acceptable: Smooth surface appearance immediately after the blink becoming irregular after a while, drying time = blink time, 3 - Good: Typical soft lens appearance with long drying time, 4 - Excellent: Appearance similar to a healthy cornea with very long drying time) | Baseline - after 2 hours of lens wear | |
Primary | Lens Wettability | Lens wettability on a 0 to 4 descriptive scale, 0.5 steps (0 - Very poor: Immediately displaying non-wetting areas on the lens surface, immediate drying time, 1 - Poor: Irregular surface appearance, drying time << blink time, 2 - Acceptable: Smooth surface appearance immediately after the blink becoming irregular after a while, drying time = blink time, 3 - Good: Typical soft lens appearance with long drying time, 4 - Excellent: Appearance similar to a healthy cornea with very long drying time) | 1 week |
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