The objective of this study is to evaluate the postoperative visual function of Taiwanese patients following bilateral or unilateral AcrySof Toric Intraocular Lens (IOL) implantation.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
56
Implantation of the AcrySof Toric Intraocular Lens (IOL)
Unnamed facility
Changhua, Taiwan
Postoperative Refractive Cylinder
Time frame: Pre-Operative Day, 1 Month Postoperative, 3 Month Postoperative
Uncorrected distance visual acuity (UCDVA)
Time frame: Pre-Operative Day, 1 Month Postoperative, 3 Month Postoperative
Best corrected distance visual acuity (BDCVA)
Time frame: Pre-operative, 1 month postoperative, 3 months postoperative
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