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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
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:
- - 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:
- - 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.
Investigator(s)
Contact us to find out if this trial is right for you.
CONTACT
Edward Manche
(650) 498-7020
View on ClinicalTrials.gov
About this Clinical Trial
Your Message Will Go To
Edward Manche6504987020