High Resolution Wavefront-guided vs. Wavefront Optimized LASIK
Trial ID or NCT#
NCT02565537
Status
NOT RECRUITING
Purpose
The investigators are comparing outcomes of LASIK surgery using a high definition wavefront-guided laser to a wavefront-optimized laser in patients with nearsightedness with and without astigmatism.
Official Title
A Prospective Randomized Comparison of the AMO CustomVue to the Alcon Wavelight in Patients Undergoing LASIK
Eligibility Criteria
Ages Eligible for Study: 21 to 60
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 -11.00 diopters with or without astigmatism of up to 5.00 diopters.
- Exclusion criteria.
- * Subjects under the age of 21.* Patients with excessively thin corneas.* Patients with topographic evidence of keratoconus.* Patients with ectatic eye disorders.* Patients with autoimmune diseases.* Patients who are pregnant or nursing.* Patients must have similar levels of nearsightedness and farsightedness in each eye. They can not be more than 1.5 diopter of difference between eyes.* Patients must have similar levels of astigmatism in each eye. They can not have more than 1.5 diopter of difference between eyes.
Exclusion Criteria:
- .
- * Subjects under the age of 21.* Patients with excessively thin corneas.* Patients with topographic evidence of keratoconus.* Patients with ectatic eye disorders.* Patients with autoimmune diseases.* Patients who are pregnant or nursing.* Patients must have similar levels of nearsightedness and farsightedness in each eye. They can not be more than 1.5 diopter of difference between eyes.* Patients must have similar levels of astigmatism in each eye. They can not have more than 1.5 diopter of difference between eyes.
Investigator(s)
Contact us to find out if this trial is right for you.
Contact
Linda Schwartz
650-724-2864
View on ClinicalTrials.gov
