Actively Recruiting

Age: 3Years - 18Years
All Genders
Healthy Volunteers
ID05770661

Axial Length Study of Children and Adolescents in Ten Provinces of China

Led by Shanghai Eye Disease Prevention and Treatment Center · Updated on 2025-12-18

30000

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

S

Shanghai Eye Disease Prevention and Treatment Center

Lead Sponsor

T

Tongji Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a large observational study to establish the normal ranges of axial length in Chinese children and adolescents. The study includes 30,000 children aged 3 to 18 years and aims to gather important eye measurements to better understand eye development and myopia progression in this population. The study involves two groups: children with myopia and children without myopia. Participants are examined using cycloplegia to collect detailed ocular data. Each child will be followed for three years with annual visits to monitor changes in axial length and eye growth. During the study, children will undergo eye assessments annually to measure axial length and its elongation over time. Researchers will collect data on ocular parameters and monitor changes to better understand eye development in myopic and non-myopic children. Participation involves regular visits over three years, and data will help establish reference standards for eye length in young people.

CONDITIONS

Brief Title

China Axial Length Study

Who Can Participate

Age: 3Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 3 to 18 years
  • Have lived in the research areas for at least one year and will not move to other places in the following two years
  • Parents or guardians sign an informed consent form
  • Children over 6 years old provide oral consent to participate
Not Eligible

You will not qualify if you...

  • Mental diseases that prevent cooperation in eye assessments
  • Ophthalmic diseases that prevent completing the eye examination

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 3 years

Participants have their axial length measured to observe changes over time.

Trial Site Locations

Total: 2 locations

1

Shanghai Eye Disease Prevention & Treatment Center

Shanghai, Shanghai Municipality, China, 200040

Actively Recruiting

2

Shanghai Eye Disease Prevention and Treatment Center

Shanghai, China

Actively Recruiting

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Research Team

X

Xun Xu, MD

X

Xiangui He, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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