Demographic information, including age and sex, was obtained via chart review. In the preoperative assessment, which occurred 1 to 3 weeks before surgery, ocular biometry, BCVA testing, IOP measurement, complete slit-lamp and fundus examination, and gonioscopy examination were performed. Intraocular pressure was measured using Goldmann applanation tonometry by a single trained ophthalmologist (SCL), and all the measurements were done during afternoon hours (2–5 PM). Gonioscopy was performed using a Zeiss-style four-mirror goniolens (model G-4; Volk Optical, Mentor, OH, USA) in low light conditions and primary position by the same ophthalmologist (SCL). The angle was graded using the Shaffer grades, and the eye was interpreted as having an occludable angle if there was a grade of 0 or 1 in at least two quadrants; otherwise, the eye was interpreted as open angle. Indentation gonioscopy was performed to rule out PAS. For ocular biometry, the LENSTAR LS 900 (Haag-Streit, Inc., Koeniz, Switzerland) was used to measure AXL, ACD, LT, and central corneal thickness (CCT). Five readings were taken for each eye. After omitting the highest and lowest values, the mean of the other three readings was used for analysis.