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Assessment of diopter variation in cycloplegia process for children with initial myopia diagnosis

Assessment of diopter variation in cycloplegia process for children with initial myopia diagnosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099732
Enrollment
Unknown
Registered
2025-03-27
Start date
2025-03-31
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Myopia

Interventions

Experimental group:Before and after ciliary muscle paralysis, subjective refraction and computerized refraction are conducted, and after the effect of ciliary muscle paralysis disappears, pupillary su

Sponsors

Eye hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 13 Years

Inclusion criteria

Inclusion criteria: 1.Aged 6-13 years, gender unrestricted; 2.Initial subjective refraction shows spherical power within [-0.50D to -2.50D], astigmatism =5.0 in each eye; 3.No congenital eye diseases, history of ophthalmic surgery, strabismus, amblyopia, nystagmus, or other ocular abnormalities; 4.Normal intraocular pressure (IOP)andslit-lamp examination.

Exclusion criteria

Exclusion criteria: 1.Positive corneal light reflex or cover test indicating manifest strabismus; 2.Best-corrected visual acuity (BCVA) 5 mmHg; 4. Ocular or systemic diseases affecting refractive status (e.g., cataract); 5.Inability to cooperate with subjective refraction procedures. 6.The subject must not participate in any other clinical trials that could influence the refractive status of the eyes.

Design outcomes

Primary

MeasureTime frame
Objective refraction diopter;Subjective refraction diopter;Best corrected visual acuity;

Secondary

MeasureTime frame
Axial length (AL);Intraocular pressure (IOP);

Countries

China

Contacts

Public ContactXinjie Mao

Eye hospital of Wenzhou Medical University

mxj@mail.eye.ac.cn+86 137 0588 0472

Outcome results

None listed

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