Skip to content

A randomized controlled trial of the effect of auricular acupoint combined with 0.01% atropine eye drops on myopia progression in myopia children

A randomized controlled trial of the effect of auricular acupoint combined with 0.01% atropine eye drops on myopia progression in myopia children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064601
Enrollment
Unknown
Registered
2022-10-12
Start date
2022-10-12
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Myopia

Interventions

Group 1:Frame glasses
Group 2:Frame glasses + atropine eye drops
Group 3:Frame glasses+auricular acupoint stimulation
Group 4:Frame glasses + atropine eye drops+auricular acupoint stimulation

Sponsors

Children’s Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 8 to 16 years children 2. 0.5% tocarbamide mydriatic optometry: -0.5DS~-6.0DS; 3. Astigmatism of less than 1.50D, anisometropia of less than 1.00D; 4. Best corrected visual acuity more than 4.9; 5. Anterior segment,position of eye, fundus, intraocular pressure are normal, intraocular pressure of 10 to 21mmHg; 6. The compliance of children and guardians is good.

Exclusion criteria

Exclusion criteria: 1. Congenital myopia caused by genetic factors; 2. Organic ocular diseases (e.g., eye infections, eyelid diseases, cataracts, congenital retinal diseases, strabismus, amblyopia), history of eye surgery, or systemic diseases; 3. Auricle deformities, ear skin defects and other ear diseases do not conform to auricular magnetic bead pressing indications; 4. History of orthokeratology lens wearing, low concentration atropine drops, and other myopia treatment; 5. Allergic to auricular tape and atropine; 6. Patients with poor treatment compliance, refusing to participate in the study or dropping out during the study; 7. Other circumstances that may affect the conduct of the clinical study and the judgment of the study results are not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Diopter;

Secondary

MeasureTime frame
Axial length;

Countries

China

Contacts

Public ContactYan Zhang

Children’s Hospital of Nanjing Medical University

82246858@qq.com+86 13912996826

Outcome results

None listed

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