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RecruitingNCT07926425ClinicalTrials.gov record

Retrospective Evaluation of Visual Outcomes, Safety and Enhancement Rates Following Wavefront-Guided LASIK Using a 10 MHz Elita Femtosecond Laser

Visual Acuity

THE QUICK READ

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 screening

Treatment, 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

Prepare your questions

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

No results are flagged as posted.

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 contactCONTACT
View location on map ↗

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

Christopher Blanton, MDCONTACTCblanton7@icloud.com408-210-5191
Official study title

Retrospective Evaluation of Visual Outcomes, Safety and Enhancement Rates Following Wavefront-Guided LASIK Using a 10 MHz Elita Femtosecond Laser

A HUMAN NEXT STEP

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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