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Evaluation of visual outcomes and patient satisfaction after wavelight plus LASIK: an ambispective, observational, multi-center study

Evaluation of visual outcomes after Wavelight Plus LASIK: an ambispective, observational, multi-center study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500107271
Enrollment
Unknown
Registered
2025-08-07
Start date
2024-12-19
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Refractive error

Interventions

Case series:none

Sponsors

Guangzhou Aier Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 35 years; 2. No significant change in refraction within the past year (periodic change within ±0.50 D); 3. Comprehensive refraction spherical equivalent no more than -10.00 D, cylindrical no more than 4.50 D, and target correction to plano; 4. Adequate corneal tissue; 5. Preoperative CDVA >= 20/25; 6. If wearing soft contact lenses before surgery, discontinue use for at least one week; if wearing rigid contact lenses, discontinue use for at least two weeks. After discontinuing contact lens wear, two comprehensive refraction results should be obtained at least one week apart, with the difference no more than 0.50 D, and the patient must sign the relevant informed consent form; 7. The patient is willing and able to comply with the follow-up schedule and relevant examinations;

Exclusion criteria

Exclusion criteria: 1. Past medical history: pterygium, viral keratitis, corneal dystrophy, glaucoma, fundus-related diseases, refractive corneal surgery, intraocular surgery, uncontrolled systemic diseases, and immune-related diseases; 2. Abnormal corneal topography indicating risk of corneal ectasia after photorefractive corneal surgery, such as keratoconus, suspected keratoconus, frustrated keratoconus, and pellucid marginal corneal degeneration; 3. Residual corneal stromal bed thickness <250µm after planned refractive surgery; 4. Preoperative dark pupil <4.5mm; 5. Special populations: such as those who are pregnant or have a mental illness.

Design outcomes

Primary

MeasureTime frame
Visual acuity;

Secondary

MeasureTime frame
refraction;axial length;Corneal topography;visual quality;subjective visual quality;

Countries

China

Contacts

Public ContactZheng Wang

Guangzhou Aier Eye Hospital

gzstwang@gmail.com+86 139 0300 2594

Outcome results

None listed

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