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A comparative study on the clinical effects of SMILE and TransPRK in the treatment of low and high myopia

A comparative study on the clinical effects of SMILE and TransPRK in the treatment of low and high myopia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121949
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-04-07
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Refractive errors

Interventions

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 16 and 60; 2. Preoperative myopia (spherical equivalent) was between -0.50 and -3.00D (low myopia group) /-6.00D or higher (high myopia group); 3. There are complete follow-up records in our hospital within one year after the operation.

Exclusion criteria

Exclusion criteria: 1. Keratoconus or suspected keratoconus; 2. Previous history of eye surgery; 3. Active eye diseases; 4. Systemic connective tissue diseases; 5. Pregnancy or lactation period; 6. The best corrected distant visual acuity (CDVA, LogMAR visual target) of the eye with poor vision is less than 0.4; 7. Non-emmetropic or monophobic treatment.

Design outcomes

Primary

MeasureTime frame
Refractive error (unaided distant visual acuity, corrected distant visual acuity, subjective spherical refraction, subjective cylindrical refraction, subjective equivalent spherical refraction);

Secondary

MeasureTime frame
Corneal morphological indicators (corneal curvature, central corneal thickness, intraocular pressure);

Countries

China

Contacts

Public ContactQianwen Gong

Eye Hospital, Wenzhou Medical University

gongqw@126.com+86 577 88068862

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026