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A multicentre study for the clinical features, visual quality and treatment of pathological myopia in China

A multicentre study for the clinical features, visual quality and treatment of pathological myopia in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024347
Enrollment
Unknown
Registered
2019-07-06
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-07-15

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

Conditions

Pathologic Myopia

Interventions

1:conbercept
2:Lucentis

Sponsors

Affiliate Eye hospital of Wenzhou Medical University; Peking University People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=40 years old; 2. Diopter =26.5mm; 3. Volunteer to participate in this observational study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. History of previous eye trauma or internal eye surgery (except cataract surgery); 2. Patients who do not cooperate with the examination can not obtain the required imaging data and related medical records; 3. Suffered with obvious mental disorders, communication or learning disabilities.

Design outcomes

Primary

MeasureTime frame
Visual acuity;—

Countries

China

Contacts

Public ContactJia Qu

Affiliate Eye hospital of Wenzhou Medical University

jqu@wz.zj.cn+86 13806898805

Outcome results

None listed

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