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Clinical efficacy of Press Needle combined with 0.01% Atropine sulfate in the treatment of low-grade myopia in children

Clinical efficacy of Press Needle combined with 0.01% Atropine sulfate in the treatment of low-grade myopia in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000393
Enrollment
Unknown
Registered
2025-02-24
Start date
2025-02-25
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

myopia

Interventions

treatment group:single vision lenses+0.01% atropine+press needle
blank control group:single vision lenses
control group:single vision lenses+0.01% atropine

Sponsors

Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1) Meet the diagnostic criteria for myopia and have normal corrected visual acuity; 2) Age 6-12 years old; 3) Refraction between -3.00D~-0.50D; no abnormality in the anterior segment of the eye and fundus examination; 4) Agree to participate in the test and sign the informed consent form by themselves and their legal guardians.

Exclusion criteria

Exclusion criteria: 1) Astigmatism = 2.00D and refractive error = 1.50D; 2) the existence of other eye diseases affecting vision such as strabismus amblyopia glaucoma cataract etc; 3) Presence of systemic diseases affecting eye health such as diabetes mellitus and hypertension; 4) History of previous eye surgery; 5) Being using other methods or participating in other studies.

Design outcomes

Primary

MeasureTime frame
spherical equivalent;axial length;

Secondary

MeasureTime frame
uncorrected distance visual acuity;fundus tessellated density;

Countries

China

Contacts

Public ContactSUN YONG

Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine

383343358@qq.com13699777775

Outcome results

None listed

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