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Myopia Control in Children: Comparison of Defocus Incorporated Multiple Segments® Lenses Versus Atropine 0.05% Eyedrops

Comparison of Defocus Incorporated Multiple Segments® (DIMS®) Lenses Alone Versus Monofocal Lenses + Atropine 0.05% Eyedrops on the Evolution of Ocular Axial Length at 2 Years in Myopia Control in Children: Single-centre Prospective Randomised Controlled 1:1 Open-label Non-inferiority Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05062031
Acronym
ATROSMART
Enrollment
116
Registered
2021-09-30
Start date
2021-10-19
Completion date
2026-02-11
Last updated
2026-08-21

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

Conditions

Myopia

Keywords

Myopia, Pediatric ophthalmology, Myopia control, Defocus Incorporated Multiple Segments (DIMS) lenses, Low concentration atropine

Brief summary

Myopia is the most common refractive disorder in the world. Many strategies have been developed to control myopia in children. Among them, the instillation of low-concentration atropine eyedrops has been proven to be effective in numerous publications. Nevertheless, the spreading of atropine use is limited by: (1) its uneven availability, (2) a proportion of children with no or poor response, (3) some issues of long-term compliance (4) the possibility of a rebound effect after treatment cessation. Among the non-drug myopia control strategies, corrective lenses including the Defocus Incorporated Multiple Segments® (DIMS®) technology have demonstrated their effectiveness in a previous study (Hong Kong) when compared to monofocal lenses. The aim of this study is to compare the efficacy of DIMS lenses alone versus atropine 0.05% eyedrops + monofocal lenses, on the evolution of ocular axial length at 2 years in myopic children.

Interventions

DEVICEDefocus Incorporated Multiple Segments® (DIMS®) lenses

Daily wear for 24 months. Lenses have a central monofocal optical zone correcting spherical or spherocylindrical ametropia, surrounded by a ring made up of 300 defocusing pellets. This lens geometry reduces the phenomenon of blurred image projected in the retinal periphery, encountered when myopic eyes are corrected with monofocal lenses.

DRUGAtropine 0.05% eyedrops

One drop each evening in both eyes for 24 months.

Daily wear for 24 months

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK
Ecouter Voir
CollaboratorUNKNOWN
Hoya Lens France
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of myopia - measured under cycloplegia - defined by: 1. A sphere power between -1 and -6 Diopters, on at least one of the two eyes 2. AND a cylindrical power strictly inferior to 2 Diopters 3. AND a maximum refractive error strictly inferior to 8 Diopters in the flattest axis * Not benefiting and never having benefited from a myopia control strategy (orthokeratology, soft defocusing lenses, low concentration atropine eye drops, peripheral defocusing corrective lenses) * Written consent of both parents

Exclusion criteria

* History of genetic disease, or general condition suggesting a syndromic myopia (including an axial length greater than 27 mm) * Strabismus * Amblyopia defined by a best corrected visual acuity strictly inferior to 10/10 on one of the two eyes * Anisometropia defined by a difference of 2 Diopters or more between the two eyes (in spherical equivalent) * History of allergy to atropine * History of severe anaphylaxis * Optical correction with contact lenses * Previous ophthalmologic surgery of the cornea, lens, retina * History of glaucoma or any other chronic ophthalmological disease in the course of treatment (including vernal keratoconjunctivitis)

Design outcomes

Primary

MeasureTime frameDescription
Axial length measurementsInclusion, 24 monthsDifference between the mean of 6 axial length measurements (in mm) acquired with the IOLMaster 500® at 24 months and the mean of 6 axial length measurements at inclusion
Spherical equivalentPre inclusion (screening consultation in the 15 days preceding inclusion), 24 monthsDifference in spherical equivalent (in diopters) under cycloplegia on autorefractometer at 24 months and at preinclusion

Countries

France

Contacts

PRINCIPAL_INVESTIGATORGilles MARTIN, MD

Hôpital Fondation Adolphe de Rothschild

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026