Clinical Trials Directory

Trials / Completed

CompletedNCT01693939

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

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Durrie Vision · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DEVICEFS200 Femtosecond Laser

Timeline

Start date
2012-02-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2012-09-26
Last updated
2013-01-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01693939. Inclusion in this directory is not an endorsement.