Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07462897

Evaluation of the Effectiveness of a New Generation of Myopia Control Lens on the Progression of Myopia in Children Aged 6 to 14 Years

The goal of this clinical investigation is to learn how much a new generation of myopia control lens (MCL1 - Myopia Control Lens 1) is helpful in reducing myopia progression in children from 6 to 14 yo. The main questions it aims to answer is: How much this new generation of lens, called MCL1, slows down the growth of the eye? Researchers will compare MCL1 to a former generation of myopia control lens (i.e. MCL2) but with better vision quality.

Participants will:

* Wear MCL1 on right eye and MCL2 on left eye for 6 months and MCL2 on rigth eye and MCL1 on left eye for the next 6 months; * Visit the hospital at 6 and 12 months for tests; * Answer weekly questionnaires on compliance wearing glasses, quality of vision and out-of-school activities.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

6 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Département d'Ophtalmologie, Hôpital Fondation Adolphe de Rothschild

Paris, 75019, France

Location status: Recruiting

Location contact

Thibaut Chapron, MD

CONTACT

[email protected]

+33.1.48.03.65.56

About this study

Myopia is a global public health issue that could affect nearly 5 billion people by 2050. It progresses rapidly in children, increasing the risk of severe ocular diseases. Several solutions exist to slow its progression, including ophthalmic lenses, which are effective and free of side effects. Essilor® Stellest® lenses, incorporating H.A.L.T. technology with aspherical lenslets, slow axial eye elongation with an efficacy comparable to high-dose atropine.

A new version of this product provides an enhanced myopia-control signal thanks to increased optical parameters of the lenslets. A recent study has demonstrated its superior effectiveness in Asian children aged 6 to 10. The present study aims to assess its performance in European children, compared with another myopia control lens, which delivers the same myopia-control signal as the original Stellest® lens but with better visual quality.

The study will take into account interindividual variability in efficacy, particularly with respect to age-a key factor in myopia progression (which is high between ages 6 and 8). Three age groups will be analyzed (6-8, 9-11, and 12-14 years). A secondary objective is to explore the impact of individual ocular parameters on lens effectiveness.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Refractive error in spherical equivalent (SE) ≤ -0.5 D and ≥ -4.5 D on each eye (autorefraction under cycloplegia)
  • Astigmatism ≤ 2.00 D for each eye
  • Anisometropia (difference in SE between the 2 eyes) ≤ 1.00 D
  • Corrected maximum distance visual acuity in each eye≥ 8/10 (equivalent to +0.1 LogMAR)
  • Written consent of the 2 holders of parental authority (or only one in the case of exclusive parental authority) and agreement of the participant

Exclusion criteria

  • Past or current use of any type of myopic control solution (braking lenses, atropine, orthokeratology, multifocal contact lenses, etc
  • Strabismus (in the test of masking near or far with the best correction)
  • Amblyopia
  • Any ocular or systemic condition known to affect refractive status (e.g., keratoconus, diabetes, Down syndrome, etc.)
  • Presence of trauma in at least one eye - Presence of inflammatory pathologies in at least one eye
  • History of intraocular surgery (cataracts, filtering surgery, intravitreal surgery) in at least one eye
  • Past or current use of growth hormones
  • Use of ocular or systemic drugs that, in the opinion of the investigator, may significantly affect pupil size, accommodation, or refractive status.
  • Wearing contact lenses
  • Allergy or intolerance to cycloplegic eye drops (cyclopentolate 0.5%)
  • Known allergy or intolerance to eyeglass frame materials
  • Children with specific visual disorders requiring personalized treatments other than conventional corrective lenses.
  • Intolerance to conventional optical corrections
  • Lack of cooperation in wearing corrective lenses

Treatment and study plan

MCL1

Device

Myopia Control Lens 1 (MCL 1) is an ophthalmic lens intended to slow down eye growth in children.

MCL2

Device

Myopia Control Lens 2 (MCL 2) is an ophthalmic lens intended to slow down eye growth in children.

Primary outcomes

  1. Change from baseline in axial length

    Time frame: 6-month

Secondary outcomes

  1. Change from baseline in cycloplegic spherical equivalent

    Time frame: 6-month

  2. Effect of optical parameters, assessed at baseline, on myopia control efficacy of MCL1 and MCL2 at 6-month.

    Time frame: 6-month

    Correlation between amount of ocular aberrations (Root Mean Square of global High Order Aberrations) at baseline and the change of eye length induced by wearing MCL1 vs MCL2 at 6-month.

  3. Effect of self-reported exposure time to natural light on myopia control efficacy of MCL1 and MCL2 at 6-month

    Time frame: 6-month

    Correlation between self-reported weekly hours of exposure to natural outdoor light, assessed with questionnaires each week and averaged at 6-month, and the change of axial length induced by wearing MCL1 vs MCL2 at 6-month.

Study contacts

Contact information is provided by the study sponsor or research team.

Thibaut Chapron, MD

CONTACT

[email protected]

00331 48 03 65 56

Sponsors and collaborators

Lead sponsor

Essilor International

Industry

Registry information

Official study title

Evaluation of the Effectiveness of a New Generation of Myopia Control Lens, Producing a Higher Myopic Control Signal Than That Produced by a Previous Generation Lens, on the Progression of Myopia in Children Aged 6 to 14 Years

Acronym: VERCORS

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Mar 10, 2026
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.