Clinical Observation of Auricular Acupressure on Prevention and Control of Myopia

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000030526

Enrollment

Unknown

Registered

2020-03-06

Start date

2020-03-09

Completion date

Unknown

Last updated

2020-03-09

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

Conditions

Myopia

Interventions

Intervention group:Auricular Acupressure

Control group:no intervention

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
Naked visual acuity;Diopter;	—

Secondary

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

Countries

China

Contacts

Public ContactXingtao Zhou

xingtaozhou@163.com+86 13816880725

Outcome results

None listed

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