Cataract Senile Clinical Trial
Official title:
Clinical Evaluation of Multifocal Intraocular Lens: OPTIVIS.TM (Evolución clínica de Lente Intraocular Multifocal: OPTIVIS.TM)
This study evaluated visual outcome after cataract surgery with bilateral implantation of either a diffractive - refractive (hybrid) multifocal intraocular lens (MFIOL) or monofocal intraocular lens (IOL) as a control grup.
PURPOSE: To present the outcomes of hybrid multifocal and monofocal intraocular lenses (IOL)
SETTING: Parc de Salut Mar, Universidad Pompeu-Fabra - Autónoma, Barcelona, Spain.
DESIGN: Prospective clinical trial.
METHODS: Consecutive patients with bilateral cataract were included. Phacoemulsification with
randomized implantation of either a monofocal IOL (AR40e, AMO-Abbot 30 Laboratories Inc.
Abbot Park, Illinois, USA) or multifocal IOL (OptiVis™, Aaren Scientific, Inc, Ontario, CA,
USA) was performed by the same surgeon and under the same conditions. Over a 3-month
follow-up, the main outcome measures were uncorrected distance visual acuity (UDVA),
corrected distance visual acuity (CDVA), uncorrected intermediate visual acuity at 60 cm
(UIVA), distance-corrected intermediate visual acuity (DCIVA), uncorrected near visual acuity
at 33 cm (UNVA), distance-corrected near visual acuity (DCNVA), spherical equivalent (SE),
contrast sensitivity (CS), presence of dysphotopsia, use of spectacles and patient
satisfaction with the test VF-14 (Visual Function Index) .
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