Clinical Research Directory

Inclusion Criteria: * Volunteer subject and guardian, fluent English spoken, willing to follow protocol and able to read, comprehend and sign the informed consent \& assent form. * Equal to or greater than 6 years and not older than 11 years at time of informed consent and assent. * Spherical equivalent refractive error (SER) by manifest refraction between -0.50 and -4.75 D in each eye. * Astigmatism, if present, of not more than 2.00 D. * Difference in SER between the two eyes (Anisometropia) by manifest refraction not more than 1.00 D. * Best corrected visual acuity in each eye better than +0.20 logMAR * Agree to wear study spectacles for at least 10 hours a day and 6 days a week * Willingness and ability to participate in trial for 1 year * Willingness and ability to attend scheduled visits * Not to involve concurrently in other myopia control treatments Exclusion Criteria: * History or presence of an Ocular disease, Strabismus, Amblyopia * Undergoing any myopia control intervention specifically Atropine and Orthokeratology * History of myopia control intervention specifically Atropine, Orthokeratology