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A Mid-to-Long-Term Clinical Study on SMILE pro for Correcting Myopic Astigmatism

A Mid-to-Long-Term Clinical Study on SMILE pro for Correcting Myopic Astigmatism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116498
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-14
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Myopia

Interventions

Control group (SMILE 3.0 group):Using Zeiss VisuMax 500 femtosecond laser to perform femtosecond laser small incision lenticule extraction surgery
Experimental group (SMILE pro group):Using Zeiss VISUMAX 800 femtosecond laser to perform femtosecond laser small incision lenticule extraction pro surgery

Sponsors

Xiangyang Eye Hospital of Aier
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age: 18 years or older. 2.Refraction: Spherical equivalent: -1.0 D to -9.0 D, Astigmatism<= 5.0 D. 3.Refractive Stability: Stable refraction for over 2 years. 4.Intraocular Pressure (IOP): <= 21 mmHg. 5.Contact Lens Discontinuation: Soft contact lenses: Discontinued for at least 1 week. 6.Rigid gas permeable (RGP) lenses: Discontinued for at least 1 month. Non-contact Tonometry Measurement: < 21 mmHg.

Exclusion criteria

Exclusion criteria: 1.History of ocular diseases, ocular surgery, ocular trauma, or systemic diseases. 2.Presence of anterior segment diseases, active pathologies, or fundus pathologies.

Design outcomes

Primary

MeasureTime frame
Naked vision;Equivalent spherical surface, ;Best corrected visual acuity;Asitigmatism;Total higher-order aberration;Spherical aberration;Coma;Trefoil;

Countries

China

Contacts

Public ContactMing Xiao

Xiangyang Eye Hospital of Aier

2295784420@qq.com+86 710 3260000

Outcome results

None listed

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