This is a clinical trial comparing an investigative accommodative IOL and two commercial IOLs in patients with cataracts undergoing primary cataract surgery.
This is a prospective, multicenter clinical study comparing the safety and performance of the Opira accommodative IOL, a commercial monofocal IOL, and a commercial multifocal IOL. Eligible patients with bilateral cataracts will undergo cataract surgery implanting one of three study lenses, and will be followed postoperatively for 24 months
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
200
The surgical procedure in which the natural crystalline lens is removed and replaced with a lens implant.
Clinica 2020
San José, Costa Rica
RECRUITINGCodet Vision Institute
Tijuana, Mexico
RECRUITINGVisual Acuity
Time frame: 6 Months
Adverse event rates
Time frame: 12 Months
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