Association of Genetic Variants With Myopia
Recruiting now
Conditions studied: Myopia
In brief
This study aims to identify genetic factors linked to myopia, including those that influence a person's risk of developing it and how quickly it progresses (like changes in eye length). It will also examine how different treatments-such as low-dose atropine drops, orthokeratology lenses, specialized glasses, and increased outdoor time-interact with these genes. Finally, the research will develop a genetic risk score to help tailor personalized myopia prevention and treatment plans.
Key facts
- Study ID
- NCT07030153
- Run by
- Beijing Visionly Plus Eye Hospital
- People needed
- 1000
- Starts
- 2025-07-01
- Expected to finish
- 2028-12-31
- Last updated by the study team
- 2025-06-22
Who can join
Age: 6 and older, up to 18. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 6-18 years.
- Any Spherical equivalent refraction (SER)
- Parental consent for genetic testing.
You may not qualify if…
- Suspected genetic syndromes (e.g., Stickler, Marfan).
- Other eye diseases (e.g., glaucoma, cataracts, retinal abnormalities, strabismus).
- Prior refractive surgery
Where it is running
- Beijing New Vision Eye Hospital — Beijing, China (enrolling)
- Beijing Visionly Plus Eye Hospital — Beijing, China (enrolling)
Full record on ClinicalTrials.gov
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