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Clinical randomized controlled trial of progressive addition lenses on the control of myopia in Chinese adolescents

Clinical randomized controlled trial of progressive addition lenses on the control of myopia in Chinese adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-07000044
Enrollment
Unknown
Registered
2007-12-12
Start date
2004-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Myopia

Interventions

Group 2:Use routine single lens as control
Group 1:Gradually focal lens

Sponsors

Zhongshan Ophthalmic Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 18 Years

Inclusion criteria

Inclusion criteria: Computer optometry after cycloplegia, binocular myopia, the spherical equivalent degree between -0.75~ -3.00D, astigmatism degree less than -1.50 D, binocular anisometropic degree less than 1.00D; Bilateral corrected visual acuity more than 1.0; Normal intraocular pressure: binocular intraocular pressure less than 21mmHg, and the difference less than 2mmHg; No history of wearing contact lenses, bifocal or multifocal lenses; Term infants, birth-weight more than 1250g; Agree to wear the lenses and follow up more than 2 years; Understand the study objective and accept the randomized allocation.

Exclusion criteria

Exclusion criteria: Manifest strabismus or other ophthalmopathy; Systematic diseases; Use of drugs that may influence the refractive status; Myopia degree of either parent more than 3D; Use of contact lenses or other myopia-treatment methods in the study.

Design outcomes

Primary

MeasureTime frame
Myopic degree;Eyeball bio-test;

Countries

China

Contacts

Public ContactZhikuan Yang
zocyang@hotmail.com+86 0 13380071988

Outcome results

None listed

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