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Clinical evaluation of periocular transcutaneous electrical acupoint stimulation (Eye-TEAS)in controlling myopia in children and adolescents:a prospective, multicenter real world study

Clinical evaluation of periocular transcutaneous electrical acupoint stimulation (Eye-TEAS)in controlling myopia in children and adolescents:a prospective, multicenter real world study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072015
Enrollment
Unknown
Registered
2023-05-31
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

myopia

Interventions

observational group:Eye-TEAS+Defocus Incorporated Multiple Segments (DIMS)
control group:Defocus Incorporated Multiple Segments (DIMS)

Sponsors

Affiliated Eye Hospital of Shandong University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1Normal near vision, naked eye far vision less than 1.0, but can be corrected with a concave lens 2 After cycloplegia spherical equivalent=-0.50D 3 Children and adolescents aged 6-18 years old 4The guardian has signed the informed consent form

Exclusion criteria

Exclusion criteria: 1Children who have combined disease with cornea, iris, crystal and fundus lesions that affect vision 2Children who have already been diagnosed with strabismus 3Children suffering from serious systemic diseases, such as cardiovascular and cerebrovascular diseases, liver, kidney, hematopoietic system and mental diseases; Allergic constitution or allergic to medical silicone; Or mental illness; 4other ocular and systemic disease abnormalities that were not considered suitable for participation in this study 5Other reasons that the study doctor considered were not suitable for inclusion in the projectwere not suitable for inclusion in the project

Design outcomes

Primary

MeasureTime frame
changes in spherical equivalent after cycloplegic;

Secondary

MeasureTime frame
changes in spherical equivalent ;changes in axial length; changes of accommodative amplitude (AMP);

Countries

China

Contacts

Public ContactHongsheng Bi

Affiliated Eye Hospital of Shandong University of Traditional Chinese Medicine

hongshengbi1@163.com+86 531 5885 9696

Outcome results

None listed

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