Clinical Trials Directory

Trials / Completed

CompletedNCT01941485

WaveLight® Refractive Flap Accuracy Study

A Prospective, Global, Multi-Center Study to Evaluate Longitudinal Flap Accuracy on Subjects Undergoing Myopic Refractive Surgery Using the WaveLight® Refractive Suite

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the accuracy of the WaveLight FS200 femtosecond laser, as assessed by 1 day and 1 month post-operative optical coherence tomography (OCT) anterior segment corneal measurements compared to pre-operative flap thickness target.

Conditions

Interventions

TypeNameDescription
DEVICEWaveLight® Refractive SuiteExcimer EX500 and Femtosecond FS200 lasers (Wavelight® Refractive Suite) used during LASIK surgery for corneal flap creation and corneal ablation
PROCEDURELASIK surgerySurgical procedure for treating refractive error based on corneal reshaping

Timeline

Start date
2013-10-01
Primary completion
2014-01-01
Completion
2015-02-01
First posted
2013-09-13
Last updated
2017-01-04
Results posted
2015-02-12

Source: ClinicalTrials.gov record NCT01941485. Inclusion in this directory is not an endorsement.

WaveLight® Refractive Flap Accuracy Study (NCT01941485) · Clinical Trials Directory