Skip to content

Clinical evaluation of different prevention and control methods for the intervention of pre-myopia in children and adolescents

Clinical evaluation of different prevention and control methods for the intervention of pre-myopia in children and adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114168
Enrollment
Unknown
Registered
2025-12-08
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Pre-myopia

Interventions

Control group:Health Education

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Equivalent spherical power: -0.50 DS < SE = 0.75 DS; 2. Astigmatism <= 1.50 D (cylindrical power); 3. Anisometropia <= 1.50 D (equivalent spherical power); 4. Corrected visual acuity of 1.0 or above; 5. Age: 6-10 years; 6. The subject and their guardian must sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Other eye diseases that affect vision; 2. Severe systemic diseases; 3. Patients with strabismus or amblyopia; 4. Currently using other methods or participating in other studies; 5. Other contraindications for both eyes, etc.

Design outcomes

Primary

MeasureTime frame
Axial Length Elongation;

Secondary

MeasureTime frame
Incidence of myopia in preclinical myopic children and adolescents at 12 months;Diopter;Best uncorrected distance visual acuity (logMAR visual acuity);Objective visual quality;Choroidal Thickness and Choroidal Capillary Density;

Countries

China

Contacts

Public ContactLi Songyu

Eye Hospital, Wenzhou Medical University

15101617011@163.com+86 571 88185600

Outcome results

None listed

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