Trials / Recruiting
RecruitingNCT07084844
Patient Reported Outcomes With WaveLight Plus LASIK
Patient Reported Outcomes and Satisfaction With Wavelight Plus LASIK
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 52 (estimated)
- Sponsor
- Mann Eye Institute · Academic / Other
- Sex
- All
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Not accepted
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 the Quality-of-Life Impact of Refractive Correction (QIRC) Questionnaire.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | WaveLigh 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
- 2025-09-05
- Primary completion
- 2026-09-01
- Completion
- 2026-09-01
- First posted
- 2025-07-25
- Last updated
- 2025-09-15
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07084844. Inclusion in this directory is not an endorsement.