Contoura With Phorcides Compared to Wavefront Optimized LASIK
Public ClinicalTrials.gov record NCT05486546. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Comparison of Visual Acuity and Quality of Life Following Contoura With Phorcides Compared to WaveLight Wavefront Optimized LASIK
Study identification
- NCT ID
- NCT05486546
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Lead sponsor
- Daniel Terveen
- Other
- Enrollment
- 120 participants
Conditions and interventions
Conditions
Interventions
- Contoura with Phorcides Procedure
- WaveLight Wavefront Optimized Device
Procedure · Device
Eligibility (public fields only)
- Age range
- 21 Years to 38 Years
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 14, 2022
- Primary completion
- Aug 31, 2023
- Completion
- Nov 30, 2023
- Last update posted
- Apr 25, 2023
2022 – 2023
United States locations
- U.S. sites
- 4
- U.S. states
- 4
- U.S. cities
- 4
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Vance Thompson Vison | Bozeman | Montana | 57105 | Recruiting |
| Vance Thompson Vision | Omaha | Nebraska | 57105 | Recruiting |
| Vance Thompson Vision | Fargo | North Dakota | 57105 | Recruiting |
| Vance Thompson Vision | Sioux Falls | South Dakota | 57108 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT05486546, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Apr 25, 2023 · Synced May 20, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT05486546 live on ClinicalTrials.gov.