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A randomized, parallel controlled trial on the effectiveness of wearing multi-point positive defocus lenses in delaying myopia in children

A randomized, parallel controlled trial on the effectiveness of wearing multi-point positive defocus lenses in delaying myopia in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052213
Enrollment
Unknown
Registered
2021-10-22
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Myopia

Interventions

Intervention group:Wearing Defocus Incorporated Multi-point Lenses
Control group:Wearing Single Vision Lenses

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 16 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 6-16 years; 2. Diopter of binocular lens: -0.75D- -7.50D; 3. Binocular astigmatism =1.0 (decimal recording method); 6. The refractive medium of the inspected eye is clear; 7. No nystagmus in both eyes, good vision fixation ability; 8. Stop wearing soft contact lenses for more than 1 week, stop wearing hard contact lenses for more than 1 month, and stop wearing orthokeratology lenses for more than 3 months; 9. Able to cooperate with various inspections.

Exclusion criteria

Exclusion criteria: 1. Strabismus, amblyopia and other eye diseases; 2. Accommodation dysfunction and/or non-strabismus binocular vision dysfunction; 3. Shallow anterior chamber, narrow angle or intraocular pressure > 21mm Hg; 4. Suffering from keratitis, pink eye, acute inflammation around the eye, glaucoma and other eye diseases; 5. Contact lens wearers (including those who wear contact lenses during the study period); 6. Any history of eye surgery; 7. Intellectual disability or mental illness; 8. Cardiopulmonary insufficiency; 9. Those with poor compliance, and the researchers believe that it is not suitable to participate in this clinical trial; 10. Participate in other lens tests at the same time.

Design outcomes

Primary

MeasureTime frame
Axial length;Diopter;

Countries

China

Contacts

Public ContactLiu Longqian
bq15651@hotmail.com+86 18980601759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026