Clinical Observation of Auricular Acupressure on Prevention and Control of Myopia

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2000003089

Enrollment

Unknown

Registered

2020-03-06

Start date

2020-03-09

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:no intervention

Intervention group:Auricular Acupressure

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Aged 8–9 years 2)Naked visual acuity > 0.8 3)The spherical equivalent of both eyes after mydriasis:-0.5DS+0.5DS 4)Cornea refractive power:40-46D 5)Good compliance and written informed consent

Exclusion criteria

Exclusion criteria: Participants who meet one of the following criteria will be excluded: 1) Suffering from other eye diseases(such as cataract, congenital retinopathy, strabismus, amblyopia, etc.) and systemic diseases. 2) Ocular pathological changes or ophthalmic surgery. 3) Participants who have used myopia prevention and control drugs (such as atropine). 4) Damaged ear skin. 5) Participants who are allergic to tape. 6) Participants who cannot cooperate with the treatment. 7) Participants whose Guardians have unreasonable expectations

Design outcomes

Primary

Measure	Time frame
Diopter;Naked visual acuity;	—

Secondary

Measure	Time frame
thickness of retina;Corneal curvature;axial length;thickness of choroid;Blood flow of related artery;Retinal blood perfusion;Choroidal blood perfusion;Accommodation;	—

Countries

China

Contacts

Public ContactXingtao Zhou

xingtaozhou@163.com+86 13816880725

Outcome results

None listed

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