NCT07127757

Clinical Evaluation of WaveLight Plus LASIK

Clinical Evaluation of Visual Outcomes With the Wavelight Plus Excimer Laser in Normal and Dim Lighting

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 50 (estimated)
• Sponsor: Laser Defined Vision · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: —

Summary

This study is a single-site, single-arm, prospective, observational study of subject satisfaction, quality of vision, and quality of life after bilateral LASIK surgery. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the adapted PROWL and Low Luminance Questionnaire (LLQ-32) Questionnaire.

Conditions

• Myopia
• Astigmatism

Interventions

Type	Name	Description
DEVICE	Wavelight Plus LASIK	Wavelight plus LASIK is an advanced laser eye surgery technology designed to enhance visual outcomes through personalized treatment plans. This system integrates comprehensive diagnostics, including biometry, tomography, and wavefront measurements, to create a tailored ablation profile for each patient.

Timeline

• Start date: 2025-08-28
• Primary completion: 2026-09-01
• Completion: 2026-09-01
• First posted: 2025-08-17
• Last updated: 2025-10-02

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study