Trials / Completed
CompletedNCT05848817
Patient Reported Satisfaction With Contoura LASIK Utilizing the Phorcides Analytic Software
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 50 (actual)
- Sponsor
- Mann Eye Institute · Academic / Other
- Sex
- All
- Age
- 21 Years – 39 Years
- Healthy volunteers
- —
Summary
The objective is to determine the percentage of subjects satisfied (Completely Satisfied or Very Satisfied) with vision after Phorcides Planned Contoura LASIK.
Detailed description
This study is a single site, single-arm, prospective, observational study of subject satisfaction, after successful bilateral LASIK surgery. Subjects will be assessed pre-operatively, operatively and at 1 week, 1 month, and 3 months post-operatively. Clinical evaluations will include measurement of visual acuity, manifest refraction, and topography, aberrometry, and administration of the OSDI and PROWL questionnaires.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Contoura LASIK | Subjects receiving Phorcides Planned Contoura LASIK |
Timeline
- Start date
- 2023-05-19
- Primary completion
- 2024-08-15
- Completion
- 2024-08-15
- First posted
- 2023-05-08
- Last updated
- 2025-07-17
- Results posted
- 2025-07-17
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05848817. Inclusion in this directory is not an endorsement.