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Evaluation of amblyopia and myopia comprehensive treatment device and traditional treatment plan on the treatment effect of amblyopia patients

Evaluation of amblyopia and myopia comprehensive treatment device and traditional treatment plan on the treatment effect of amblyopia patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096835
Enrollment
Unknown
Registered
2025-02-07
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Amblyopia

Interventions

Experimental group:The synthetic amblyopia treatment instrument and monocular occlusion
Control group:Red light glitter and monocular occlusion

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged more than or equal to 6 years old and less than or equal to 10 years old, specifically 6 years old =1.50D or the difference in astigmatism is >=1.5D0D, and the difference in the best corrected visual acuity between the two eyes is greater than or equal to more than 2 lines; normal visual acuity in the contralateral eye (5-point visual acuity>=5.0 or logMar visual acuity<=0); 3. Those who are willing to participate in this clinical verification and can cooperate with the completion of the entire trial process; 4. No history of visual training and not during visual training treatment; 5. Eye health, no organic eye disease.

Exclusion criteria

Exclusion criteria: 1) Suffering from eye diseases, such as acute or chronic inflammation of the eyes, history of glaucoma, etc; 2) poor compliance and inability to cooperate with training and treatment; 3) Individuals who cannot undergo regular eye examinations; 4) Hyperopia is greater than+10.00D, or astigmatism with the rules is greater than 4.50D in accordance with the rules, or astigmatism against the rules is greater than 1.50D; 5) Phoria is greater than 10 degrees with glasses at near or in distance.

Design outcomes

Primary

MeasureTime frame
Vision acuity;

Secondary

MeasureTime frame
Accommodative facility and amplitude;Contrast sensitivity test;

Countries

China

Contacts

Public ContactWang Yuwen

Eye Hospital, Wenzhou Medical University

wyw-0721@163.com+86 13868440619

Outcome results

None listed

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