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Safety and Effectiveness of CARE1.02 Spectacle Lens in Myopia Control

Safety and Effectiveness of CARE1.02 Spectacle Lens Versus Single-vision Spectacle Lens in Myopia Control: a Randomised Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05818033
Enrollment
796
Registered
2023-04-18
Start date
2023-04-25
Completion date
2025-06-12
Last updated
2026-03-12

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

Conditions

Myopia

Keywords

Myopia control

Brief summary

China is a major country in myopia, with the highest number of teenagers suffering from myopia. Controlling the progression of myopia and the related complications caused by axial elongation have clinical significance and social value. Currently. There is a lack of researches on the impact of specially designed myopia control spectacle lens in adolescents aged 12 and above. Therefore, The researchers plan to conduct a randomized controlled trial among myopia adolescents aged 12-17 in middle and high schools in Guangzhou, to test and verify the safety and effectiveness of CARE1.02 on myopia control compared with single-vision spectacle lens.

Interventions

DEVICECARE1.02

Participants in the intervention group will wear CARE1.02 and receive the follow-up checks.

Participants in the control group will wear single-vision spectacle lens and receive the follow-up checks.

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Aged 12 to 17 years; * Under the condition of bilateral cycloplegic autorefraction, the spherical refractive error of -0.50 to -8.00 D in each eye and astigmatism of not more than 1.50 D and anisometropia of not more than 1.50 D; * Best-corrected visual acuity of equal or better than 0.00 LogMAR (\>= 1.0 as Snellen). * The intraocular pressure of 10 to 21mmHg. * Volunteer to participate in this clinical trial with signature of the informed consent form.

Exclusion criteria

* History of eye injury or intraocular surgery; * Clinically abnormal slit-lamp findings; * Abnormal fundus examination; * Ocular disease, such as uveitis and other inflammatory diseases,glaucoma, cataract, fundus diseases, eye tumors, dominant strabismus, and any eye diseases that affect visual function; * Systemic diseases causing low immunity (such as diabetes, Down's syndrome, rheumatoid arthritis, psychotic patients or other diseases that researchers think are not suitable for wearing glasses); * Participation of the drug clinical trial within three month and the device clinical trial within one month; * Only one eye meets the inclusion criteria; * Unable to have regular follow-up; * Participation of any myopia control clinical research trial within three months, and currently using rigid contact lenses (including nursing products), multifocal contact lenses, progressive multifocal lenses and other specially designed myopia control lenses, atropine drugs, etc.

Design outcomes

Primary

MeasureTime frameDescription
Changes of spherical equivalent refraction (SER) at one year1 yearThe difference of SER at one year from baseline. SER will be measured after cycloplegia

Secondary

MeasureTime frameDescription
Best corrected visual acuity at one year1 yearBest corrected visual acuity
Binocular visual function at one year1 yearBinocular visual function
Choroidal thickness at one year1 yearThe difference of Choroidal thickness at one year from baseline.
Visual scale score at 1 year1 yearVisual scale score measured by the Chinese version of the pediatric refractive error profile2 (PREP2)
Changes of axial length (AL) at one year1 yearThe difference of AL at one year from baseline.
Change of anterior chamber depth (ACD) at one year1 yearThe difference of ACD at one year from baseline.
Change of lens thickness (LT) at one year1 yearThe difference of LT at one year from baseline.
Change of corneal curvature (CR) at one year1 yearThe difference of CR at one year from baseline.
Time length of wearing spectcales at one year1 yearTime length of wearing spectcales collected every half year
Safty of wearing the spectacle lens1 yearSafty of wearing the spectacle lens which is a qualitative outcome will be evaluated every half year by prespecified measures and definations through symptoms and signs, intraocular pressure#slit lamp and ocular fundus checks.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026