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.
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Investigator(s)

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

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Contact

Edward Manche
6504987020

View on ClinicalTrials.gov