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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)
Edward Manche
Refractive surgery specialist,
Cornea specialist
Professor of Ophthalmology at Stanford University Medical Center
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