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Patient Reported Outcomes With WaveLight LASIK

NCT06668909 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2026-03-23

Study results available
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Summary

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.

Conditions

  • Myopia

Interventions

DEVICE

WaveLight® EX500

Phorcidies Planned Contoura LASIK

Sponsors & Collaborators

  • Sengi

    collaborator INDUSTRY

  • OVO LASIK + Lens

    lead OTHER

Eligibility

Min Age
21 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-01
Primary Completion
2025-02-14
Completion
2025-02-14
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06668909 on ClinicalTrials.gov