An Outcomes Study Comparing the Intralase FS 60 to the Intralase iFS When Performing LASIK Surgery for Nearsightedness

Trial ID or NCT#

NCT01365728

Status

not recruiting iconNOT RECRUITING

Purpose

The purpose of the study is to compare the results of LASIK surgery when using two versions of a femtosecond laser in patients with nearsightedness with and without astigmatism.

Official Title

A Prospective Randomized Comparison of Fellow Eyes Undergoing LASIK With the Intralase FS 60 Versus the Intralase IFS

Eligibility Criteria

Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: Yes
Inclusion Criteria:
  1. * Subjects age 21 and older with healthy eyes.* Nearsightedness between -0.25 diopters and -7.00 diopters with or without astigmatism of up to 3.00 diopters.
    1. Exclusion Criteria:
  2. * Subjects under the age of 21.* Patients with excessively thin corneas.* Patients with topographic evidence of keratoconus.* Patients with ectactic eye disorders.* Patients with autoimmune diseases.
Exclusion Criteria:
  1. * Subjects under the age of 21.* Patients with excessively thin corneas.* Patients with topographic evidence of keratoconus.* Patients with ectactic eye disorders.* Patients with autoimmune diseases.
View All Criteria
Show Less

Contact us to find out if this trial is right for you.

Contact

Edward Manche
6504987020

View on ClinicalTrials.gov