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Clinical Trial Summary

The objective is to evaluate the resultant thickness of the FS200 created LASIK flap compared to plan at the surgical visit.


Clinical Trial Description

This study is a Single site, single-arm, prospective, observational study of the accuracy of the intended flap thickness, after successful bilateral LASIK surgery. Subjects will be assessed pre-operatively, operatively and at 1 day post-operatively. Clinical evaluations will include measurement of visual acuity, manifest refraction, and flap thickness, and flap diameter. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05501795
Study type Observational
Source Bismarck Lasik
Contact
Status Completed
Phase
Start date August 9, 2022
Completion date January 19, 2023

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