Retrospective Evaluation of Visual Outcomes, Safety and Enhancement Rates Following Wavefront-Guided LASIK Using a 10 MHz Elita Femtosecond Laser
Visual Acuity
What this study involves
The registry says this study is recruiting. Individual locations may have different availability.
- Study type
- Observational
- Phase
- Not applicable / not listed
- Age range
- 18 years - Not specified
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 175 Estimated
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
The goal of this retrospective chart review is to evaluate the effectiveness of a 10MHz femtosecond laser utilized in performing wavefront-guided LASIK in a myopic population. Our hypothesis is that the outcomes will be as good as if not better than previous myopic LASIK outcomes.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
Inclusion Criteria:
Consecutive eyes with myopia or myopic astigmatism Underwent wavefront-guided LASIK At least 6-12 months of follow up
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Exclusion Criteria:
Uncontrolled systemic or ocular disease, No prior ocular trauma or surgery, Visual acuity less than 20/20 Ocular pathology affecting visual acuity Abnormal pupils Inability to obtain wavefront measurements Contact lens wear within 7 days prior to surgery
Study population
Myopic and myopic astigmatism patients
Understand screeningTreatment, groups and participation
The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.
- Assignment
- Not reported
- Masking
- Not reported
Myopic LASIK candidates
Not reported in this registry record.
Procedure: eye surgery · Device: Femtosecond LASER
eye surgery PROCEDURE
Wavefront guided LASIK surgery
Femtosecond LASER DEVICE
10 MHz femtosecond laser for flap formation
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
Visual Acuity
Time frame: 6-12 months post-op
Snellen chart
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (1)
The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.
1 locations
Pacific Eye IsntituteRancho Cucamonga, California, United StatesRecruiting
Study team and timeline
- Lead sponsor
- CB Consulting
- Study start
- Nov 4, 2026 Actual
- Primary completion
- Jan 31, 2027 Estimated
- Study completion
- Jan 31, 2027 Estimated
- First posted
- Nov 9, 2026 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
Official study title
Retrospective Evaluation of Visual Outcomes, Safety and Enhancement Rates Following Wavefront-Guided LASIK Using a 10 MHz Elita Femtosecond Laser
Ask Wellness Clinical Research
Your message goes to WCR, including when this study is run by another organization. WCR may offer general guidance but may not operate this trial, have access to its team or be able to enroll you.
Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026
