To prospectively evaluate postoperative visual and refractive parameters in a series of subjects bilaterally implanted with AcrySof ReSTOR +3 vs. those bilaterally implanted with LENTIS MPlus Intraocular Lens (IOL).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
24
Bilateral implantation of an Alcon AcrySof ReSTOR +3 Intraocular Lens (IOL) Model SN6AD1 following cataract extraction.
Bilateral implantation of a LENTIS MPlus Intraocular Lens (IOL) following cataract extraction.
Contact Alcon Call Center for Trial Locations
Oviedo, Principality of Asturias, Spain
Unilateral Uncorrected Near Visual Acuity
Time frame: 3 months after surgery
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