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.
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

Investigator(s)

Edward Manche, MD
Edward Manche, MD
Ophthalmologist
Professor of Ophthalmology

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

Contact

Edward Manche
6504987020

View on ClinicalTrials.gov