“…Patients were required to be at least 21 years of age and have myopic refractive error between ÿ1.00 and ÿ7.00 diopters (D), with less than ÿ3.00 D of astigmatism (measured via cycloplegic subjective refraction). 7 Patients were excluded from participating in this trial if (1) they had a difference in high-contrast visual acuity of 4 or more letters between eyes, (2) visual acuity worse than 20/32 in either eye, (3) spherical anisometropia more than 1.00 D, (4) cylindrical anisometropia more than 0.75 D, (5) an intended ablation that would leave an estimated corneal thickness less than 250 mm, (6) anterior segment pathology or previous ocular surgery, or (7) a history of systemic autoimmune disease or immunosuppressive therapy, or were pregnant or lactating. Hydrogel lens wearers were required to discontinue lens wear 2 weeks before surgery, and rigid gas-permeable lens wearers were required to discontinue wear 3 weeks before surgery.…”