An Evaluation of Myopia Control Lenses on Wearing Experience in Myopic Children
An Evaluation of Visual Comfort, Adaptation and Overall Satisfaction in Myopic Children Using A.M.L. Series of Lenses
Essilor International
40 participants
Jan 2, 2026
INTERVENTIONAL
Conditions
Summary
The goal of this research study is to understand the wearing experience of A.M.L. series of lenses in myopic children. The main questions it aims to answer are: * How quickly and effectively children adapt to the A.M.L. series of lenses? * The proportion of children who adapted to the A.M.L. series of lenses within 4 to 6 days? 40 myopic children aged 6 to 12 years will be recruited as participants, and all of them will be wearing A.M.L. series of lenses. Participants will: * Wear A.M.L. series of lenses for a period of 2 weeks * Visit at day 4-6, week 1 and week 2.
Eligibility
Inclusion Criteria8
- 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 Criteria9
- 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
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Interventions
Participants will be wearing A.M.L. series of lenses for a period of 2 weeks.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07354945