The objective of the study is to compare clinical outcomes from PRK and SBK using FDA-approved laser technology in the same patient
Patients undergoing bilateral laser refractive surgery on the same day will be randomly assigned to have one eye treated with PRK and the fellow eye treated with SBK.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
University of Utah, John Moran Eye Center
Salt Lake City, Utah, United States
Visual acuity
Time frame: 6 months
Manifest refraction
Time frame: 6 months
Wavefront aberration value
Time frame: 6 months
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