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Clinical Trial Summary

The purpose of this study is to collect efficacy and safety data on the WaveLight EX500 excimer laser system for the correction of hyperopia with and without astigmatism by laser in situ keratomileusis (LASIK) treatment.


Clinical Trial Description

Qualified subjects will receive LASIK treatment in both eyes and be followed for 1 year. Subjects will be asked to attend a total of 9 visits (Screening, Surgery, Day 1, Week 1, Month 1, Month 3, Month 6, Month 9, and Month 12). Total expected duration of subject participation is approximately 1 year. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04805593
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date April 28, 2021
Completion date May 2, 2023

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