Serafilcon A contact lenses
DeviceReusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection
Other names: LID022821
NCT Number: NCT05431478
The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Drs. Giedd, PA, Maitland, Florida, United States
In this crossover study, subjects will wear each study lens type for approximately 14 days and attend 7 scheduled visits. The expected duration of subject participation in the study is approximately 28 days (approximately 14 days per each study lens type).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection
Other names: LID022821
Reusable silicone hydrogel contact lenses worn during the day and removed at night for daily cleaning and disinfection
Other names: ACUVUE OASYS® 2 Week with HYDRACLEAR® PLUS, AOHP
Hydrogen peroxide based contact lens cleaning and disinfecting solution
Other names: CLEAR CARE® Cleaning and Disinfecting Solution
Time frame: Week 1, each wear period. A wear period was approximately 14 days.
Visual acuity (VA) was assessed with study lenses in place using logarithmic of the Minimum Angle of Resolution (logMAR) charts. A logMAR acuity of 0.0 corresponds to 20/20 Snellen acuity (normal visual acuity), with a negative value denoting better than 20/20 visual acuity. Each eye was assessed individually. No hypothesis testing was pre-specified for this endpoint.
Alcon Research
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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