Trials / Completed
CompletedNCT06668909
Patient Reported Outcomes With WaveLight LASIK
Patient Reported Outcomes on Vision Quality and Dry Eye Following Treatment With Wavelight LASIK
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 300 (actual)
- Sponsor
- OVO LASIK + Lens · Academic / Other
- Sex
- All
- Age
- 21 Years – 35 Years
- Healthy volunteers
- —
Summary
This study is a multi-site, single-arm, ambispective, observational study of subject satisfaction, after successful bilateral LASIK surgery. Subjects will be assessed 12+ months post-operatively. Clinical evaluations will include administration of the OSDI, modified PROWL, and dry eye questionnaires.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | WaveLight® EX500 | Phorcidies Planned Contoura LASIK |
Timeline
- Start date
- 2024-11-01
- Primary completion
- 2025-02-14
- Completion
- 2025-02-14
- First posted
- 2024-11-01
- Last updated
- 2026-03-23
- Results posted
- 2026-03-23
Locations
4 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06668909. Inclusion in this directory is not an endorsement.