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Effect of wearing defocused soft contact lens on myopia progression and visual correlation in children and adolescents with myopia

Effect of wearing defocused soft contact lens on myopia progression and visual correlation in children and adolescents with myopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064731
Enrollment
Unknown
Registered
2022-10-15
Start date
2022-10-15
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

myopia

Interventions

Group 1:Concentric defocus soft contact lens
Group 2:Single vision glasses (spectacles)

Sponsors

West China hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 8 and 12 years old; 2. Myopia increased by at least -0.50D/year in the first 12 months before entering the study; 3. The spherical diopter is between -0.75 and -4.00 D; 4. Astigmatic diopter=0.8 (decimal recording method); 7. The refractive medium of the tested eye is clear; 8. The tested eye has no nystagmus and good fixation ability; 9. The corneal curvature is between 40.00 D and 46.00 D.

Exclusion criteria

Exclusion criteria: 1. Cardiopulmonary insufficiency or systemic diseases; 2. Suffering from intellectual development disorders or mental related diseases; 3. Taking medication; 4. Have a history of eye surgery; 5. Suffering from diseases such as strabismus, glaucoma, cataracts that may affect eye growth and development; 6. Has there been any recent occurrence of eye inflammation, infection, or trauma, severe eye discomfort, or systemic or eye diseases that affect contact lens wearing (such as dry eye syndrome); 7. Have worn contact lenses; 8. Using myopia control measures or preparing to use other myopia control measures; 9. Being or preparing to participate in other lens tests; 10. Shallow anterior chamber or intraocular pressure>20mmHg; 11. Insufficient regulation or aggregation; 12. In a dark environment, the pupil is smaller than the minimum diameter required for measuring 6mm aberration; 13. Due to poor compliance, the researchers believe that it is not appropriate to continue participating in this clinical trial.

Design outcomes

Primary

MeasureTime frame
axial length;subjective refraction;

Secondary

MeasureTime frame
objective refraction;corneal endothelial;visual acuity;aberration;accommodative power;corneal topography;relative peripheral refraction;

Countries

China

Contacts

Public ContactLiu Longqian

West China Hospital, Sichuan University

liulq@scu.edu.cn+86 18980601759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026