Study of Method for Early Diagnosis of High Myopia

Clinical study on prevention and treatment of pathological myopia and its associated complications using the method of integrative medicine

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100043026

Enrollment

Unknown

Registered

2021-02-04

Start date

2021-02-19

Completion date

Unknown

Last updated

2021-05-24

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

Conditions

Myopia

Interventions

myopic children group:No intervention

Eligibility

Sex/Gender

All

Age

No minimum to 16 Years

Inclusion criteria

Inclusion criteria: 1. The subjects who signed the informed consent; 2. Subjects under 16 years old; 3. Subjects with - 6.00D < equivalent spherical diopter <= - 1.00d after mydriasis.

Exclusion criteria

Exclusion criteria: 1. Subjects with pathological myopia related fundus lesions. 2. Subjects who could not cooperate well due to poor mental state; 3. Subjects with other systemic diseases such as hypertensive retinopathy and diabetic retinopathy were excluded.

Design outcomes

Primary

Measure	Time frame
diopter;	—

Secondary

Measure	Time frame
corneal curvature;	—

Countries

China

Contacts

Public ContactBi Hongsheng

Shandong University of Traditional Chinese Medicine Affiliated ophthalmology hospital

hongshengbi@163.com+86 13953113696

Outcome results

None listed

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