Condition: Myopia · Astigmatism · Sponsor: Laser Defined Vision
This study is a single-site, single-arm, prospective, observational study of subject satisfaction, quality of vision, and quality of life after bilateral LASIK surgery. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the adapted PROWL and Low Luminance Questionnaire (LLQ-32) Questionnaire.
This description comes directly from the study's public registry record.
Carrie Williams · 336-288-8823 · ldv2020@gmail.com
Always discuss trial participation with your own doctor first.
| Laser Defined Vision | Greensboro, North Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07127757