Patient Reported Outcomes With WaveLight LASIK

Completed

Conditions studied: Myopia

In brief

This study is a multi-site, single-arm, ambispective, observational study of subject satisfaction, after successful bilateral LASIK surgery. Subjects will be assessed 12+ months post-operatively. Clinical evaluations will include administration of the OSDI, modified PROWL, and dry eye questionnaires.

Key facts

Study ID

NCT06668909

Run by

OVO LASIK + Lens

People needed

300

Starts

2024-11-01

Expected to finish

2025-02-14

Last updated by the study team

2026-03-23

Who can join

Age: 21 and older, up to 35. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Wavefront Optimized or Phorcidies Planned Contoura LASIK for myopia or myopic astigmatism 12 to 15 months ago
• Age: 21 to 35 years of age at the time of surgery.
• Preoperative myopic sphere of -1.00 D to -8.00 D
• Preoperative regular astigmatism of 0.00 D to -3.00 D.
• Stable refraction preoperatively defined as < 0.5 D of change over at least 1 year.
• Refractive target of bilateral emmetropia.

You may not qualify if…

• Corneal ectatic disorders.
• Patients with a calculated residual stromal depth of < 300 um.
• Pre-existing retinal or corneal pathology, or irregular astigmatism.
• Pre-existing autoimmune diseases, dry eye, glaucoma, diabetes, etc.
• Previous corneal surgeries prior to LASIK.
• LASIK enhancements.

Where it is running

• NVISION Eye Centers — San Diego, California, United States
• Boston Vision — Brookline, Massachusetts, United States
• Ovo Lasik + Lens — Saint Louis Park, Minnesota, United States
• Mann Eye Institute — Houston, Texas, United States

Full record on ClinicalTrials.gov

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