Skip to content

A multicenter real-world observational study on pathological myopia

A multicenter real-world observational study on pathological myopia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600131461
Enrollment
Unknown
Registered
2026-09-02
Start date
2026-10-01
Completion date
Unknown
Last updated
2026-09-07

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

Conditions

pathologic myopia

Interventions

Group with simple high myopia:None
Tractional maculopathy:None
Atrophic macular degeneration:None

Sponsors

Hebei Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The informed consent form has been signed; 2. Age >=14 years old and =26.5mm.

Exclusion criteria

Exclusion criteria: 1. Severe refractive media ambiguity makes it impossible to perform fundus photography or OCTA testing; 2. Other ophthalmic diseases: diabetic retinopathy, central plasma disease, retinal arteriovenous occlusion, uveitis, keratitis, etc. 3. Regular follow-up visits cannot be made.

Design outcomes

Primary

MeasureTime frame
Axis oculi;

Secondary

MeasureTime frame
Optic disc structural parameters;Diopter;Mean Deviation;Pattern Standard Deviation;Intraocular pressure;

Countries

China

Contacts

Public ContactWang Lifei

Hebei Eye Hospital

wlfhb@126.com+86 319 3237196

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026