Can a new lens design keep Kids' eyesight sharp?
NCT ID NCT07779941
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This study tests whether ZEISS MyoActive lenses, designed to send a specific optical signal to the eye, can prevent or delay the onset of short-sightedness (myopia) in children who are not yet myopic but are at risk. Children aged 6 to 12 with mild farsightedness will be randomly assigned to wear either these special lenses or standard single-vision glasses for 12 months. Researchers will track changes in their eye measurements and vision to see if the lenses slow eye growth and reduce the chance of becoming myopic.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ZEISS MyoActive spectacle lenses
- What this could lead to
- If effective, these lenses could offer a simple, non-invasive way to prevent or delay myopia onset in children, reducing future risks of high myopia and related eye conditions.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. The lenses may not prevent myopia, and there could be unknown side effects or discomfort.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 124 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2029
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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6 to 12 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria Participants enrolled in the trial must: 1. be accompanied by a parent or guardian who is able to read and comprehend English and sign a record of informed consent/assent; 2. be able to understand and participate in the Assent process; 3. at baseline, be within the age range of 6 to 12 years old inclusive; 4. No prior spectacle correction 5. Cycloplegic spherical equivalent (SE) 0.00 to + 2.00 D 6. Astigmatism of less than -1.50D 7. Anisometropia of not more than 1.50D 8. At least 1 parent or more with myopia Exclusion Criteria Participants enrolled in the trial must NOT have: * Any pre-existing systemic or ocular condition, including infection or disease that is likely to affect visual acuity and refractive error; * Any systemic disease that adversely affects ocular health e.g. diabetes, Graves disease, and auto-immune diseases such as ankylosing spondylitis, multiple sclerosis, Sjögrens syndrome and systemic lupus erythematosus. * Use of or a need for any systemic medication or topical medications which may alter normal ocular findings / are known to affect a participant's ocular health / physiology in an adverse or beneficial manner at enrolment and/or during the study. NB: Systemic antihistamines are allowed on an "as needed basis", provided they are not used prophylactically during the trial and at least 24 hours before the study product is used. * History of eye trauma * Amblyopia * Strabismus * History of any form of optical correction * Any concomitant myopia control treatment including atropine eyedrops, contact lenses or other myopia control glasses. The Investigator may, at their discretion, exclude anyone who they believe may not be able to fulfil the study requirements or it is believed to be in the participant's best interests.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Singapore National Eye Centre
Singapore, Singapore
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- LASIK gets a precision upgrade to sharpen night vision
- A daily eye drop might slow childhood nearsightedness. a trial puts it to the test.
- Can a single lens implant restore near and distance vision?