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Enrolling by invitation NCT07119723

Environmental Factors and Myopia Prevalence Among Uyghur Students in Remote China

Observational Myopia Environment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Myopia, Environment. Basic parameters: 6 years — 15 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Ophthalmologic screening performs annually. Main information collected: gender, age, race, school, visual acuity, autorefractive results.

Primary outcome measures

  • spherical equivalent refraction [Time frame: From January 2020 to December 2026]

Eligibility criteria

Inclusion criteria

  • 6 -15 years old

Exclusion criteria

  • Students with strabismus, amblyopia, or other ocular diseases.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Tianjin medical university eye hospital — Tianjin

Identifiers

NCT: NCT07119723 · 20240902

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗