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Inhibition of Myopia Progression With Optical Devices

Inhibition of Myopia Progression With Optical Devices

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07698977
Enrollment
50
Registered
2026-07-13
Start date
2026-06-02
Completion date
2027-05-31
Last updated
2026-07-13

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

Conditions

Myopia, Myopia, Child Myopia Progression, Myopia Progression

Keywords

myopia, myopia progression, optical device, DIMS lenses, bulbar axial length

Brief summary

This observational study aims to determine whether optical devices designed to slow myopia progression and/or environmental factors can prevent myopia progression in the pediatric and adolescent myopic population. The study aims to answer the following questions: 1. How does myopia progression change with age while wearing myopia progression control glasses? 2. How does myopia progression change while wearing myopia progression-control glasses when environmental factors, such as time spent outdoors and place of residence, are taken into account? 3. How does myopia progression change at different ages while wearing myopia progression control glasses given a family history of myopia? This will be a self-controlled observational study. Participants who are myopic after cycloplegic refraction will be prescribed DIMS glasses. DIMS stands for "defocus incorporated multiple segments," a specialized optical technology used in spectacle lenses to slow nearsightedness progression in children. Patients will keep a diary of their subjective symptoms and environmental factors, e.g., time spent outdoors and screen time. Patients will visit the clinic once every six months for checkups and the following tests: * Best corrected visual acuity test * Stereopsis * Automatic refractometry * Bulbar axial length measurement In a follow-up study, researchers will compare myopia progression with environmental and baseline factors to learn about the long-term effects of DIMS lenses on myopia progression.

Detailed description

As an observational study we aim to examine the effects of D.I.M.S. lens's daily wear on myopia progression in relation to the environmental factors. Our pediatric and adolescent myopic population is selected as follows: Inclusion Criteria: * Participants must be between 6 and 15 years of age at the start of myopia progression treatment * Caucasian ethnicity * Refractive error measured under cycloplegia, expressed as spherical equivalent: between -0.50 Dsph and -10.0 Dsph * Wearing myopia-control glasses during waking hours * Willing to Participate in follow-up examinations up to 24 weeks Exclusion criteria: * pathological myopia (e.g., myopia onset before age 6, Stickler syndrome) * preterm infants born before 32 weeks of gestation * previous eye-opening surgery (e.g., lens extraction) * Traumatic eye injury * Known connective tissue disorder (e.g., Marfan syndrome) * Irregular or improper use of progressive-lens glasses * Failure to attend the follow-up examinations scheduled In the self-controlled observational study the myopic participants are wearing during day time DIMS glasses. DIMS stands for "defocus incorporated multiple segments," a specialized optical technology used in spectacle lenses to slow nearsightedness progression in children. DIMS glasses not only correct the refractive errror but also provide a circular defocus zone to avoid periferial retinal defocus. Patients will keep a diary of their subjective symptoms and environmental factors, e.g., time spent outdoors and screen time, subjective symptoms. Patients will visit the clinic once every six months for checkups and the following tests: * Best corrected visual acuity test * Stereopsis * Automatic refractometry * Bulbar axial length measurement These measurements and tests are part of the regular ophthalmological follow-up examinations. The study aims to answer the following questions: 1. How does myopia progression change with age while wearing myopia progression control glasses? 2. How does myopia progression change while wearing myopia progression-control glasses when environmental factors, such as time spent outdoors and place of residence, are taken into account? 3. How does myopia progression change at different ages while wearing myopia progression control glasses given a family history of myopia? Statistical analysis plan includes non-parametric t-test, one way and two way ANOVA tests.

Interventions

DEVICEWearing myopia-control D.I.M.S. glasses while awake

DIMS (Defocus Incorporated Multiple Segments) lenses wearing while awake

DEVICEDIMS (Defocus Incorporated Multiple Segments) lenses

D.I.M.S. lenses are worn like normal glasses to correct myopia and, beyond that, their special design is intended to slow myopia progression via defocus lenslets. There is targeted myopic defocus produced by the mid-peripheral lenslets with positive power to inhibit eye length growth.

Sponsors

Semmelweis University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* • Participants must be between 6 and 15 years of age at the start of myopia progression treatment * Caucasian ethnicity * Refractive error measured under cycloplegia, expressed as spherical equivalent: between -0.50 Dsph and -10.0 Dsph * Wearing myopia-control glasses while awake * Participation in follow-up examinations every 6 months

Exclusion criteria

* • Pathological myopia (e.g., myopia onset before age 6, Stickler syndrome) * Premature birth before the 32nd week of gestation * Previous eye-opening surgery (e.g., lens removal) * Traumatic eye injury * Known connective tissue disorder (e.g., Marfan syndrome) * Irregular or improper use of progressive-lens glasses * Failure to attend the follow-up examinations scheduled every 6 months

Design outcomes

Primary

MeasureTime frameDescription
Best corrected visual acuity testup to 24 weekZero is equivalent to no vision and 1.0 indicates the best visual acuity in decimal scale. Distance and near visual acuity is measured under standard conditions
Bulbar axial length measurementup to 24 weekIt is defined as the distance from the anterior surface of the cornea to the retinal pigment epithelium, measured in millimeters using optical device. An increase in axial length is characteristic of the elongation of the eye.

Secondary

MeasureTime frameDescription
Stereopsisup to 24 weekstereopsis test (depth perception test) measures how well the eyes create three-dimensional vision. The precision of depth perception is measured in seconds of arc (arcsec) using a test plate. If stereoscopic vision is present, the smaller the angle, the more refined the stereopsis.

Countries

Hungary

Contacts

CONTACTZoltan Zs Nagy, Professor
szem.titkarsag@gmail.com+3614591500
CONTACTAmarilla Barcsay-Veres
veres.amarilla@semmelweis.hu+3614591500
PRINCIPAL_INVESTIGATORZoltan Zs Nagy, Professor

Semmelweis University Ophthalmology Department

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 14, 2026