New contact lenses aim to curb childhood myopia epidemic
NCT ID NCT07547085
First seen Jun 25, 2026 · Last updated Sep 18, 2026 · Updated 3 times
Summary
This study tests two types of daily disposable contact lenses designed to slow the progression of myopia (nearsightedness) in children aged 7 to 12. Over two years, 126 Hong Kong Chinese children will wear either a special lens or a standard single-vision lens, with their eyes measured every six months. The goal is to see if these lenses can reduce how fast their eyesight gets worse.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- daily disposable contact lenses with peripheral myopic defocus
- What this could lead to
- If successful, these lenses could offer a simple way to slow down worsening nearsightedness in children, reducing their risk of severe eye problems later in life.
- What could go wrong
- This is a relatively small, early-stage trial (126 children) and results may not apply to all kids. The lenses might not slow myopia as hoped, and there is a risk of discomfort or eye infections with contact lens wear.
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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 126 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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7 to 12 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * • Age at enrolment: 7 - 12 (both inclusive) years old Hong Kong Chinese schoolchildren * Refractive errors in terms of spherical equivalent refraction (SER) determined by cycloplegic autorefraction: -0.75 diopters (D) to -5.00D in both eyes * Astigmatism: equal or less than -1.00D * Anisometropia: equal or less than -1.75D * Previous myopia progression: * -0.50D (in SER) per year or more in 1 eye or both eyes OR Axial length elongation: 0.27mm/year in 1 eye or both eyes * If myopia is initially detected during screening, eligibility requires an SER below the 3rd percentile curve of refraction in either or both eyes (4) * Best corrected visual acuity: better than 0.04 LogMAR in both eyes * Ocular health: no abnormalities in both internal and external ocular health * Systemic health: no systemic interference with ocular vision functioning * Binocular vision: no strabismus and other binocular abnormalities * No medication or supplements that affect eye growth * Normal colour vision * No previous use of myopic control interventions such as red-light therapy, atropine, orthokeratology, specialized spectacle lenses and contact lenses and oral supplements for myopic control * Agree to maintain the visit schedule and be able to keep all appointments as specified in the informed assent and consent forms throughout study duration. * Agree to accept either the control or study lens as assigned by the randomization scheme * Agree to wear the assigned contact lenses for a minimum of 10 hours per day, at least 6 days per week, for the duration of the 2-year study and to inform the study investigator if this schedule is interrupted. Wearing time may be modified by the study staff for health reasons * Agree to adhere to contact lens use requirements throughout study duration * Acceptance of the masked study design Exclusion Criteria: * Contraindications for soft contact lenses * Dry eye with drug intervention within 30 days * Regular use of ocular medication (prescription or over-the-counter), artificial tears, or wetting agents due to dryness, allergies or other conditions that hinder the contact lens wear * Current use of systemic medications that may significantly affect contact lens wear, tear film production, pupil size, accommodation, or refractive state. These include, but not limited to, long term use of nasal decongestants (e.g., pseudoephedrine, phenylephrine), antihistamines (e.g., chlorpheniramine, diphenhydramine, Prednisolone or Ritalin (methylphenidate) * Pre-existing systemic and ocular disease that had an influence on contact lens wearing * History of ocular injury or surgery * Prior use of myopic control interventions such as red-light therapy, atropine, orthokeratology, specialized spectacle lenses and contact lenses and oral supplements * Allergy to cyclopentolate eye drops * Subjects who, in the judgment of the Investigator, are unable to cooperate and follow instructions during eye examination
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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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Optometry Research Clinic, School of Optometry, The Hong Kong Polytechnic University
RECRUITINGKowloon, Hong Kong, Hong Kong
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- Can glasses that slow nearsightedness also reshape a Child's astigmatism?