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Evaluation of the Post-LASIK Flap Thickness of the FS200 Femtosecond Laser Flap

Myopia Clinical Trial

Official title:
A Single Center Prospective Evaluation of the Post-LASIK Flap Thickness of the FS200 Femtosecond Laser Flap

Clinical Trial Summary

The purpose of this study is to document the programmed flap thickness to achieved flap thickness using the FS200 femtosecond laser in performing LASIK procedure. The FS200 Femtosecond laser is a precision surgical device that is used to create a flap in a FDA approved LASIK procedure.

Clinical Trial Description

The objective of this study is to evaluate the thickness of the corneal flap created with the FS 200 Femtosecond laser flap during the LASIK procedure using the Visante and OptiVue OCT ultrasound devices. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01693939
Study type Interventional
Source Durrie Vision
Contact
Status Completed
Phase Phase 4
Start date February 2012
Completion date April 2012
View Details
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