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Effects of peripheral retinal hyperopia defocus lenses on ocular biology and visual function in children with pathological hyperopia

Effects of peripheral retinal hyperopia defocus lenses on ocular biology and visual function in children with pathological hyperopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121232
Enrollment
Unknown
Registered
2026-03-27
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Hyperopia

Interventions

Test group:Wear peripheral farsighted defocus lenses

Sponsors

Nanjing Tongren Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Age: 6-12 years; 2. Binocular lens power + 3.00 ~ + 7.50 d, cylindrical lens power 0 ~-2.00 d 3. Dioptric Anisometropia was less than 1.50 d, cylindrical anisometropia was less than 1.00 d 4. Best-corrected visual acuity 40/50 or higher.

Exclusion criteria

Exclusion criteria: 1. History of eye trauma or surgery 2. Shallow anterior chamber or intraocular pressure >21mmHg 3. Clinical abnormalities found in ophthalmic slit-lamp examination 4. Significant eye diseases such as keratitis, conjunctivitis, acute periocular inflammation, or glaucoma 5. Manifest strabismus 6. Systemic diseases or other conditions deemed unsuitable 7. Participation in another clinical trial within the past 3 months 8. Poor compliance, unwillingness to follow up 9. Considered by the investigator as unsuitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Axial eye;diopter;vision;

Secondary

MeasureTime frame
intraocular pressure;

Countries

China

Contacts

Public ContactZixiu Zhou

Nanjing Tongren Hospital

54178593@qq.com+86 180 6880 0989

Outcome results

None listed

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