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Based on Multispectral Refraction Topography optical interventions for myopia control

Based on Multispectral Refraction Topography optical interventions for myopia control

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066890
Enrollment
Unknown
Registered
2022-12-21
Start date
2022-12-23
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

1.2:-
2.1:-
3.1:optical defocus spectacle
3.2:optical defocus spectacle
4.1:orthokeratology
4.2:orthokeratology
1.1:-

Sponsors

Eye Hospital, WMU,Hangzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 17 Years

Inclusion criteria

Inclusion criteria: Part 1: 1) Children aged 6-17 with myopia;2) Equivalent spherical lens: 0 to -8.00D;3) Corrected visual acuity =0.8;4) Intraocular pressure of 10-21mmHg; Part 2: 1) Children aged 6-17 with myopia;2) Equivalent spherical lens: 0 to -8.00D;3) Corrected visual acuity =0.8;4) Intraocular pressure of 10-21mmHg; Part 3: 1) Age: 6-17 years old;2) Equivalent spherical degree of computer optometry in binocular cycloplegia: -0.75D to -5.00D;Binocular astigmatism =1.50D;Best corrected visual acuity =1.0 Part 4: 1) Children with myopia aged 6 ~ 17 years;2) Diopter of -0.75 ~ -4.00D, astigmatism of 0-1.50D, anisometropia =1.00D;3) Corrected visual acuity =1.0;4) Visual acuity =0.8 after wearing glasses;5) The K value of cornea was in the range of 39.00-46.00D;6) Intraocular pressure of 10-21mmHg;

Exclusion criteria

Exclusion criteria: Part 1: 1) Wear history of lenses with myopia control without OK lens, defocusing frame, defocusing soft lens 2) No history of 0.01% atropine use;3) Other serious ocular diseases with refractive errors and ocular surgical history were excluded; Part 2: 1) Wear history of lenses without OK lens, defocusing frame, defocusing soft lens and other myopia control lenses;2) No history of 0.01% atropine use;3) Other serious ocular diseases with refractive errors and ocular surgical history were excluded; Part 3: 1) History of eye surgery and trauma;Have strabismus, glaucoma and other eye diseases (except ametropia);History of systemic disease;2) Used drugs related to myopia control and prevention and control measures (such as low-concentration atropine eye water, multi-point myopia defocusing lens, orthokeratology lens, etc.);3) Poor fit or unqualified image quality. Part 4: 1) Wear history of lenses without OK lens, defocusing frame, defocusing soft lens and other myopic control lenses;2) No history of 0.01% atropine use;3) Obvious dry eye symptoms;4) Severe conjunctivitis;5) Other serious ocular diseases with refractive errors and ocular surgical history were excluded;Exit criteria: The patient will quit midway due to subjective or objective reasons, and the follow-up examination and review items will not be carried out;

Design outcomes

Primary

MeasureTime frame
Diopter;anteroposterior axis;

Secondary

MeasureTime frame
OCTA;Vision quality;peripheral refraction;

Countries

China

Contacts

Public ContactChenRuru

Eye Hospital, WMU,Hangzhou

251517129@qq.com+86 13868051650

Outcome results

None listed

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