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Keratoconus for perceptual learning

A randomized controlled clinical study of perceptual learning improving visual function in patients with keratoconus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056395
Enrollment
Unknown
Registered
2022-02-05
Start date
2022-02-04
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

keratoconus

Interventions

Intervention group:Glasses perceptual learning training
Control group:Glasses placebo training

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged 9 years or older; 2. Has been diagnosed as Keratoconus, BAD-D >= 2.6; 3. Change of Kmax < 1.0d and change of BAD-D < 0.4175 betweem the last two Pentacam result; 4. The best corrected visual acuity of both eyes was between 0.1 and 1.0; 5. Has voluntarily agreed to participate in the study by signing the statement of informed consent.

Exclusion criteria

Exclusion criteria: 1. Has history of acute keratoconus; 2. Has other eye diseases or other diseases/conditions causing vision loss; 3. Has eye surgery history; 4. Currently using local/systemic medications or other interventions that may affect visual function; 5. Receiving other treatments that may affect the results of this study, such as contact lenses during the study; 6. Has any known neurological diseases; 7. Participating in other studies currently that may affect the results of this study; 8. Study other reasons that the physician considers inappropriate for inclusion in the program.

Design outcomes

Primary

MeasureTime frame
Distant best corrected visual acuity;

Secondary

MeasureTime frame
Distant uncorrected visual acuity;

Countries

China

Contacts

Public ContactYang Xiao

Zhongshan Ophthalmic Center, Sun Yat-Sen University

Yangx_zoc@163.com+86 13760664837

Outcome results

None listed

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