An interventional study of Investigational Myopia Control Spectacle Lens and Single Vision Spectacle Lens in Myopia and Myopia Progression, sponsored by Essilor International. Not yet recruiting at 1 site in Singapore. Open to participants aged 6 Years to 10 Years. Per ClinicalTrials.gov, last updated 2026-09-24.
Sponsored by Essilor International · Not applicable, Interventional, and Treatment
The purpose of this clinical trial is to compare a new myopia control spectacle lens with a standard single vision spectacle lens in slowing the progression of myopia (nearsightedness) in healthy children aged 6 to under 11 years.
The main question being studied is:
Is the new myopia control spectacle lens more effective than a standard single vision spectacle lens in slowing myopia progression?
In this study, participants will wear a myopia control spectacle lens in one eye and a standard single vision spectacle lens in the other eye for the first 6 months. The lens assignment will then be switched between eyes for the remaining 6 months. Researchers will compare changes in eye axial length and refractive error between the two lens types.
Participants will:
1,159 studies on the registry are indexed under Myopia; 225 are open to participants now.
This study's planned enrollment of 20 is below the median of 78 across 923 interventional studies indexed under Myopia.
Browse Myopia studies →Essilor International is the lead sponsor of 38 studies on the registry; 20 are open to participants now.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants will wear the investigational myopia control spectacle lens in the left eye and a standard single vision spectacle lens in the right eye for the first 6 months. After 6 months, the lens assignment will be switched, with each eye wearing the opposite lens type for another 6 months.
Device: Investigational Myopia Control Spectacle Lens · Device: Single Vision Spectacle Lens
Participants will wear the investigational myopia control spectacle lens in the right eye and a standard single vision spectacle lens in the left eye for the first 6 months. After 6 months, the lens assignment will be switched, with each eye wearing the opposite lens type for another 6 months.
Device: Investigational Myopia Control Spectacle Lens · Device: Single Vision Spectacle Lens
A spectacle lens designed to help slow the progression of myopia in children
A standard spectacle lens used to correct refractive error without a specific myopia control feature
Change in Eye Axial Length
Time frame: From baseline to 6 months
Change in Eye Axial Length
Time frame: From 6 months to 12 months
Change in Eye Non-Cycloplegic Spherical Equivalent Refraction
Time frame: From baseline to 6 months
Change in Eye Non-Cycloplegic Spherical Equivalent Refraction
Time frame: From 6 months to 12 months
Plan to share: No
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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