Clinical Research Directory

Inclusion Criteria: Age between 18 to 40 years * Willing to use the prescribed soft daily disposable contact lenses * Normal ocular health * Rx range from +8.00 to -12.00DS and up to 2.50DC (within range that could be fitted by CV 1 day CLs) * Willing to provide written consent in English * Can attain good vision: Best-corrected visual acuity of 6/12 or better in each eye * Have no history of ocular surgery, injury, recent or current infection within the last 3 months * Have no known allergies to the study products * Willing to attend the scheduled study visits and adhere to instructions * If taking fish oil or tear supplements, should have started at least 3 months prior to starting the study and not planned changes to supplement intake during the study Exclusion Criteria: * RGP, Extended Wear (re-usable), presbyopic, therapeutic/cosmetic, or myopia control contact lens wear * Experienced contact lens wearer with a history of regular lens wear more than 3 months * Unstable refractive error * Binocular vision anomaly not controlled by contact lenses * Patients require Presbyopic correction or age more than 40 years * Age \< 18 years old * Not on a stable medication * Participation in another clinical trial within 2 weeks of participation in this study * History or presence of any ocular disorder or condition in either eye that would likely interfere with the interpretation of the study results or patient safety * Self-reported pregnancy or lactation * Any ocular or systemic condition that may contradict contact lens wear \*\* \*The investigator has the right to exclude any patient's participation in the study if he/she deems it to be in the best interest of the patient. Minor exceptions to the inclusion / exclusion criteria will be submitted to, and considered by, the Pl and approved as required. This includes 'drop-outs' that subsequently return to contact lens wear during the study trial. * OO/CLO (ECP) Clinical Judgement