A multicenter randomized controlled study on the prevention and control of children's pseudomyopia to true myopia

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2000004031

Enrollment

Unknown

Registered

2020-10-22

Start date

2020-11-01

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Myopia

Interventions

Control group:Health education

Trial group:Health education + appropriate techniques (pinch acupuncture + ear acupoint pressing)

Eligibility

Sex/Gender

All

Age

6 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Equivalent spherical mirror power: - 0.50ds < equivalent spherical mirror; 2. People aged 6-10 years; 3. The subject who signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with other eye diseases that affect vision; 2. Patients with serious systemic diseases; 3. Strabismus and amblyopia; 4. The subjects with one or both parents, monocular or binocular high myopia (equivalent spherical lens < - 6.00ds); 5. Subjects who are using other methods or participating in other studies.

Design outcomes

Primary

Measure	Time frame
spherical equivalent;	—

Secondary

Measure	Time frame
Corneal curvature;Adjustment range;Eye axis;Best distance vision with naked eyes;	—

Countries

China

Contacts

Public ContactZefeng Kang

Ophthalmic Hospital of Chinese Academy of Traditional Chinese Medicine

zefeng2531@163.com+86 13552597717

Outcome results

None listed

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