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Genetic mutation screening in families with early onset high myopia

Genetic mutation screening in families with early onset high myopia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075313
Enrollment
Unknown
Registered
2023-09-01
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

early onset high myopia

Interventions

Case series:NA

Sponsors

Hangzhou Campus of Wenzhou Medical University Affiliated Eye and Optometry Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 30 Years

Inclusion criteria

Inclusion criteria: (1) A clear diagnosis of high myopia (myopia greater than -6.00 diopter or eye axis length 26mm); (2) The age of onset was less than 7 years old

Exclusion criteria

Exclusion criteria: (1) Patients with high myopia in only one eye; (2) Patients with high myopia caused by external reasons such as visual deprivation and drugs; (3) Neither parent can provide genetic information.

Design outcomes

Primary

MeasureTime frame
Subjective refraction;Objective refraction;axial length;Macular thickness;fundus photo;choroidal thickness;

Countries

China

Contacts

Public ContactLI FENFEN

Eye Hospital of Wenzhou Medical University

lifenfen_wzmu@163.com+86 151 6779 9221

Outcome results

None listed

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