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Clinical study of acupuncture in preventing and controlling the progression from pseudomyopia to true myopia in children

Clinical study of acupuncture in preventing and controlling the progression from pseudomyopia to true myopia in children

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100055087
Enrollment
Unknown
Registered
2021-12-31
Start date
2021-06-01
Completion date
Unknown
Last updated
2023-01-09

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
Experimental group:health education + acupuncture treatment

Sponsors

The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Subjects with at least one eye meeting the above diagnostic criteria: spherical equivalent power: -0.00DS < spherical equivalent <-0.50DS; 2. Aged 6 to 10 years (including 6 years old and 10 years old); 3. The refractive interstitium of both eyes is clear, and the organic diseases of the eye are excluded; 4. The subject children and their families can understand and be willing to receive treatment and review according to the experimental protocol; 5. Sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Combined with age-related macular degeneration, glaucoma, diabetic retinopathy, retinal arterial/venous occlusion, idiopathic or secondary epimacular membrane, choroidopathy, optic nerve disease (optic neuritis, optic atrophy), macular hole, strabismus, amblyopia and other eye diseases that affect the test results; 2. The test eye has undergone intraocular surgery within 3 months; 3. Those who have participated in clinical trials of any drug or medical device within 12 weeks before the trial, or those who plan to participate in other clinical trials during this trial; 4. Those who are afraid of acupuncture; 5. Severe systemic disease, moderate or severe liver dysfunction, or severe heart, lung, renal dysfunction, hematopoietic system disease and mental illness; 6. Those who cannot cooperate with the inspection and treatment process; 7. One or both parents have high myopia in one or both eyes (equivalent spherical lens <-6.00DS).

Design outcomes

Primary

MeasureTime frame
Naked eye vision;Equivalent spherical mirror;Ocular axis;Corneal curvature;

Secondary

MeasureTime frame
Adjustment amplitude;

Countries

China

Contacts

Public ContactGao Wen

1. The First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine 2. National Clinical Research Center of Traditional Chinese Medicine and Acupuncture and Moxibustion

gaowenxiuwen@163.com+86 18622300583

Outcome results

None listed

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