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Clinical Study of SMILE 4.0-VISULYZE in Correcting Refractive Errors
Sponsor: Affiliated Hospital of Nantong University
Summary
The aim of this study is to further optimize the surgical input parameters for patients undergoing Small Incision Lenticule Extraction (SMILE) using the regression model established by the SMILE 4.0-VISULYZE system, thereby achieving satisfactory postoperative refractive outcomes. In this study, patients scheduled for SMILE surgery at the investigators' hospital will be divided into two groups: a conventional group, where the input parameters are adjusted based on historical experience according to the patient's refractive error, and a 4.0-VISULYZE group, where the input parameters are optimized using the SMILE 4.0-VISULYZE system. The investigators will compare the postoperative outcomes between the two groups, including uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), spherical power, cylindrical power, spherical equivalent (SE), and the proportions of patients achieving postoperative visual acuity ≥0.8, ≥1.0, and ≥1.2 at 1 day, 10 days, 1 month, 3 months, 6 months, and 1 year post-surgery. Additionally, the investigators will evaluate the proportions of patients with postoperative SE within ±0.50D and ±1.0D, as well as postoperative cylindrical power within ±0.50D and ±1.0D, to assess the efficacy and safety of the SMILE 4.0-VISULYZE system in treating refractive errors.
Key Details
Gender
All
Age Range
18 Years - 40 Years
Study Type
INTERVENTIONAL
Enrollment
600
Start Date
2024-11-01
Completion Date
2026-12-31
Last Updated
2025-05-28
Healthy Volunteers
No
Interventions
Group 4.0-VISULYZE
The 4.0-VISULYZE group had their infusion rates precisely calibrated using 4.0-VISULYZE
traditional group
The traditional group had their infusion rates based on past experience.
Locations (2)
The Affiliated Hospital of Nantong University
Nantong, Jiangsu, China
The Affiliated Hospital of Nantong University
Nantong, Jiangsu, China