NCT07926425 · CB Consulting
Retrospective Evaluation of Visual Outcomes, Safety and Enhancement Rates Following Wavefront-Guided LASIK Using a 10 MHz Elita Femtosecond Laser
What this study is about
The goal of this reviewing past data 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.
View original scientific description
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.
Interventions
PROCEDURE
eye surgery
Wavefront guided LASIK surgery
DEVICE
Femtosecond LASER
10 MHz femtosecond laser for flap formation
Primary outcome measures
Visual Acuity
Time frame: 6-12 months post-op
Snellen chart
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Consecutive eyes with myopia or myopic astigmatism undergoing wavefront-guided LASIK with at least 6 to 12 months of follow-up -
Exclusion criteria
- Uncontrolled systemic or ocular disease, 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 \-
Where
- Rancho Cucamonga, California
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Nov 12, 2026 · Source of record for eligibility and locations