Back to search results

WaveLight Plus LASIK for Myopia and Astigmatism

This study is looking at how satisfied people are with their vision after having WaveLight Plus LASIK surgery. WaveLight Plus LASIK is a type of laser eye surgery that uses advanced technology to create a personalized treatment plan for each person. The study wants to see how satisfied you are with your uncorrected vision (vision without glasses or contacts) three months after the surgery. You might be able to join if you are between 18 and 39 years old, have myopia (nearsightedness) and/or astigmatism (blurry vision at all distances), and meet other standard requirements for LASIK. The study is currently unclear on its recruitment status.

Study design
This is an observational study, meaning researchers will watch and record information without giving specific treatments. It will involve 52 participants at one location.
What's involved
You will have WaveLight Plus LASIK surgery and then be assessed up to 3 months afterward. This will include checking your vision and answering questionnaires about your satisfaction and quality of life.
Compensation
Not stated in the trial record.
Follow-up
Participants will be assessed up to 3 months after their surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07084844

Patient Reported Outcomes With WaveLight Plus LASIK

Recruiting
Not specifiedAges 18–39Observational
Mann Eye Institute
~52 participants
Updated 2025-09-15 on ClinicalTrials.gov
What's tested:WaveLigh Plus LASIK

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Mean score of satisfaction with uncorrected vision after wavelight plus LASIK based on PROWL-SS Questionnaire preoperative vs postoperative (question #1 [Q1] only).
Measured over 3 months postoperative

Conditions

Myopia
Astigmatism

Explore related trials

AstigmatismMyopia

Where it's being run

1 sites across 1 states
Texas1

Study leadership

  • Phillip Brunson · PRINCIPAL_INVESTIGATOR · Mann Eye Institute

Who to contact

Study Coordinator
[email protected]
713-580-2500 · ext. 2389
Email the study team

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Between the ages of 18 and 39
Meet the standard care requirements for LASIK
Spherical equivalent (SE) more than -1.00D and up to -9.00 diopters
Myopia ≤ -8.00 sphere (in minus cylinder format) and up to -3.00D astigmatism
SE difference between the manifest refraction and the Sightmap measured SE being less than 0.75D
Minimum residual stromal bed thickness of 250 µm
If currently wearing contact lenses:
Soft CTL wearers discontinue for minimum 3 days
RGP CTL wearers discontinue for 1 month per decade of wear
Stable refraction (2 consecutive manifest refractions within 0.25 SE)
Stable K readings (2 consecutive K readings in 2 consecutive visits)
Willing and able to complete all post-operative visits
Pre-surgery BCDVA of 20/20 (0.00 logMAR) or better in each eye.Mesopic pupil size ≥ 4.5mm

Exclusion

Subjects with any prior ocular surgery
Subjects with topographic evidence of keratoconus, or ectasia
Subjects with autoimmune diseases
Subjects who are pregnant or nursing
Systemic disease likely to affect wound healing, such as diabetes and severe atopy
Any ocular disease (including un-controlled dry eye) which in the investigator's opinion would affect the outcome of refractive surgery

What this trial measures

  • Mean score of satisfaction with uncorrected vision after wavelight plus LASIK based on PROWL-SS Questionnaire preoperative vs postoperative (question #1 [Q1] only).3 months postoperative