Visual improvement effect of visual cortex training on patients after SMILE surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900025650

Enrollment

Unknown

Registered

2019-09-04

Start date

2019-09-01

Completion date

Unknown

Last updated

2019-09-09

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

Conditions

Myopia

Interventions

Training group:Do the isual cortex RevitalVision visual training

Eligibility

Sex/Gender

All

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) age 18-40 years, regardless of gender; 2) more than 3 months after SMILE surgery; 3) patients with unsatisfactory operation effect and low contrast sensitivity; 4) residual SPH <= -1.50d, CYL <= -1.00d; 5) sign informed consent and volunteer to participate in this study.

Exclusion criteria

Exclusion criteria: 1) patients with postoperative corneal dilatation or keratoconus; 2) subject's activities are limited due to illness, medication or emotional state; 3) have migraine or epilepsy; 4) subjects who are currently participating in other studies and may directly or indirectly affect the results of this study; 5) previous mental illness.

Design outcomes

Primary

Measure	Time frame
vision;	—

Secondary

Measure	Time frame
Contrast sensitivity;	—

Countries

China

Contacts

Public ContactJiping Xu

Zhongshan Ophthalmic Center of Sun Yat-Sen University

842051098@qq.com+86 18260989609

Outcome results

None listed

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