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A Monocentre, Randomized, Contralateral Trial to Study the Effect of Temporal Changes in Ocular Biometry of Two Myopia Control Lenses

A Monocentre, Randomized, Contralateral Trial to Study the Effect of Temporal Changes in Ocular Biometry of Two Myopia Control Lenses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111940
Enrollment
Unknown
Registered
2025-11-07
Start date
2025-11-12
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Interventions

Arm 1:Right eye: Myopia Control Lens 1 (MCL 1)
Left eye: Myopia Control Lens 2 (MCL 2) Each participant wears the study eyeglasses containing both Myopia Control Lens 1 (MCL 1) and Myopia Control Lens 2 (MCL 2) design.
Arm 2:Right eye: Myopia Control Lens 2 (MCL 2)
Left eye: Myopia Control Lens 1 (MCL 1) Each participant wears the study eyeglasses containing both Myopia Control Lens 1 (MCL 1) and Myopia Control Lens 2 (MCL 2) design.

Sponsors

Essilor International
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1. Volunteer participant 2. Informed consent of parent or guardian and assent of participant 3. Age: Equal to or greater than 6 years but not older than 13 years at the time of informed consent and assent 4. Refractive error (manifest refraction): Equal or less than -0.50 D or equal or greater than -4.75D 5. Astigmatism should be less than or equal to 2.00D 6. Anisometropia should be less than or equal to 1.00D 7. Best corrected visual acuity: Better than 0.20 logMAR in each eye 8. Willingness and ability to participate in trial for at least 6 months and attend scheduled visits 9. Not to be involved in other myopia control treatments concurrently 10. No history of any myopia control interventions (i.e., myopia control spectacle lenses, myopia control contact lenses, orthokeratology lenses or atropine, etc.)

Exclusion criteria

Exclusion criteria: 1. History or presence of an ocular disease, strabismus or amblyopia 2. Currently or previously on any myopia control interventions (i.e., myopia control spectacle lenses, myopia control contact lenses, orthokeratology lenses or atropine, etc.)

Design outcomes

Primary

MeasureTime frame
Change in axial length;

Secondary

MeasureTime frame
Change in choroidal thickness;

Countries

Singapore

Contacts

Public ContactAparna Gopalakrishnan

Essilor International

aparna.gk@essilor.com+65 6293 6801

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026