Clinical Research Directory

Inclusion Criteria: * Volunteer participant * Informed consent of parent/guardian and assent of participant * Age equal to or greater than 6 years and not older than 12 years at the time of signing informed consent and assent * Spherical equivalent refraction (SER) by cycloplegic autorefraction equal or less than -0.50 D and equal or greater than -4.75D with astigmatism not more than 2.00 D on both eye * Difference in SER (anisometropia) between two eyes should not exceed 1.50 D * Best corrected visual acuity (BCVA) better than or equal to +0.10 LogMAR in each eye * Be in good general health, based on the participant and the parent's/guardian's knowledge * Willingness and ability to participate in study and comply with all scheduled visits Exclusion Criteria: * History of Atropine, Orthokeratology, or Red Light treatment * Strabismus by cover test at near or distance wearing correction * Amblyopia * Any ocular or systemic condition known to affect refractive status (e.g. keratoconus, diabetes, Downs syndrome, or other developmental disorders, etc.) * Current use of ocular or systemic medications which, in the investigator's opinion, may significantly affect pupil size, accommodation or refractive state * History of ocular injury or surgery * Participation in any clinical study within 30 days of the Baseline visit * Study participants deemed inappropriate for the study by the investigator * The inherent ocular/systemic discomfort (dry eyes, visual fatigue, headaches, etc.) that may affect the evaluation of the study lens wearing experience, from the investigator's perspective