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Effects of different correction methods on the prevention and control of low-grade myopia

Juvenile myopia prediction based on axial biological parameters and machine learning algorithms

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049050
Enrollment
Unknown
Registered
2021-07-20
Start date
2021-07-20
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

myopia

Interventions

Group 1:single vision spectacle lenses
Group 2:placebo
Group 3:orthokeratology

Sponsors

Shandong Eye Instiute, Qingdao Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. The spherical diopter of the patient is -0.50D~-6.00D and the cylinder diopter is less than -1.00D after mydriasis and optometry; 2. The patient's age is between 6 and 18 years old; 3. The patient's best corrected visual acuity is 1.0 or above; 4. Patients need to voluntarily sign the informed consent; 5. Patients should be able and willing to follow up on time during the study period.

Exclusion criteria

Exclusion criteria: 1. The patient has underlying, recurrent or progressive corneal disease and corneal abnormalities (especially recurrent corneal erosion, severe stromal disease, keratoconus, and hyaline marginal keratosis); 2. The patient has irregular corneal morphology in one or both eyes; 3. The patient is taking some systemic drugs that may affect the refraction, such as adrenocortical hormones and antimetabolites; 4. The patient is immunocompromised or has connective tissue disease, dominant genetic disease or diabetes; 5. The patient has a history of eye surgery; 6. The patient's central corneal curvature is irregular; 7. The patient is allergic to the drugs used in the study; 8. The patient has a history of glaucoma or suspected glaucoma; 9. The patient participates in other trials during the trial; 10. The patient has a history of herpetic keratitis; 11. The patient uses local or systemic drugs to control the progression of myopia; 12. The patient suffers from nystagmus or is unable to fixate for long periods of time during surgery.

Design outcomes

Primary

MeasureTime frame
axial length;subjective refraction;Peripheral retinal defocus;Biomechanics;aberration;

Countries

China

Contacts

Public ContactLeng Lin

Shandong Eye Instiute, Qingdao Eye Hospital

coollin.1987@163.com+86 18661800680

Outcome results

None listed

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