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Clinical Trials in Singapore / NCT07533149
Recruiting Not applicable

Targeted Lens Intervention for Myopic Anisometropia in Children

NCT07533149 · tracked via the Priya Life Science Singapore tracker
Phase
Not applicable
Started
2026-08-13
Last updated
2026-09-15

Condition(s) studied

AnisometropiaMyopia

Investigational drug(s) / intervention(s)

More myopic eye: MCL1; Less myopic eye: MCL2

More myopic eye: MCL1; Less myopic eye: MCL2: Each participant wears the study eyeglasses containing both Myopia Control Lens 1 (MCL1) and Myopia Control Lens 2 (MCL2) design, with one type of lens in each eye throughout the study period. MCL1 will be worn in the more myopic eye, and MCL2 in the less myopic eye for a period of 12 months.

Study summary

The goal of this clinical trial is to learn if our research spectacles will lower the difference in prescription (spectacles degree) between the eyes in children between 6 to 13 years old with anisometropic myopia. Anisometropic myopia is when the difference in myopia prescription between the two eyes are more than 1 diopter. The main question it aims to answer is:

* How the eye responds to the research spectacles over time by measuring:

1. Change in axial length: the physical length of the eye from front to back.
2. Change in cycloplegic spherical equivalent refraction: an accurate measurement of the eye's prescription taken while the focusing muscles are temporarily relaxed with eye drops.

Participants will:
* Wear the study spectacles
* Visit Essilor R\&D Centre and an eye clinic for follow-up sessions

Eligibility

Sex
ALL
Min age
6 Years
Max age
13 Years
Healthy volunteers
No
Inclusion Criteria: 1. Voluntary 2. Informed consent of parent/guardian and assent of participant 3. Age equal to or greater than 6 years old and less than 13 years at the time of signing informed consent and assent 4. SER equal or less than -0.50 D and equal or greater than .5.00 D with astigmatism not more than 2.50 D 5. Difference in SER (anisometropia) between two eyes .1.00 D 6. Best corrected visual acuity (BCVA) better than or equal to +0.20 LogMAR in each eye 7. Agree to wear study spectacles for .12 hours/day and 7 days/week 8. Willingness and ability to participate in investigation for 12 months and attend scheduled visits punctually 9. Agree for no concurrent involvement in other myopia control treatment Exclusion Criteria: 1. History or presence of an ocular disease affecting refractive status 2. History or presence of strabismus 3. Presence of amblyopia 4. Current or previous use of atropine and/or orthokeratology 5. Known allergy to cycloplegic agents 6. Contraindication to cycloplegic agents 7. Cognitive or psychological vulnerability

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Essilor R&D Centre Singapore Singapore Singapore Recruiting

More Essilor International trials in Singapore

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07533149 on ClinicalTrials.gov ↗ ← All trials in Singapore