Primary Effectiveness Sample Clauses
Primary Effectiveness. The primary objective of this study is to evaluate the overall performance of DD T2 lenses when compared to Oasys 1-Day, MyDay and 1-Day Acuvue Moist. The primary endpoint is the subjective rating on overall quality of vision, collected binocularly on a scale of 1 (Poor) to 10 (Excellent).
Primary Effectiveness. The primary objective of this study is to evaluate the overall performance of an investigational silicone hydrogel contact lens over 2 weeks of daily wear. The primary endpoint is front surface wettability, collected on a 5-point scale, for each eye.
Primary Effectiveness. The primary objective of this study is to explore overall vision with BIOFINITY ENERGYS as compared to BIOFINITY lenses after 1 week of wear. The primary endpoint is the subjective rating of overall vision, collected binocularly on a scale of 1 (Poor) to 10 (Excellent).
Primary Effectiveness. The primary objective of this study is to evaluate the overall performance of an investigational silicone hydrogel lens when compared to AOHP. The primary endpoint is distance VA with study lenses, collected in logMAR, for each eye.
Primary Effectiveness. The primary objective of this study is to evaluate the clinical performance of an investigational frequent replacement daily wear SiHy sphere contact lens, , over 7 days of daily wear. The primary endpoint is front surface wettability, collected on a 5-point scale, for each eye.
Primary Effectiveness. The primary objective of this study is to evaluate corneal staining observed after 2 hours of wear with LID018869 against both PureVision, pre-cycled with Biotrue, and Biofinity lenses, pre-cycled with Replenish. The primary endpoint is the average of corneal staining areas observed (expressed as a percent) taken over the 5 regions: central, superior, nasal, inferior, and temporal, after 2 hours of lens wear.
Primary Effectiveness. The primary objective of this study is to evaluate the overall performance of PRECISION1 contact lenses when compared to INFUSE contact lenses. The primary endpoint is distance VA with study lenses, collected in logMAR, for each eye.
Primary Effectiveness. The primary objective of this study is to evaluate VA after approximately 4 weeks of lens wear. The primary endpoint is distance VA with study lenses, collected in Snellen at the 4-week follow-up visit, for each eye. Conversion will be made to the logMAR scale.