Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocular Lens (IOL)

Alcon Research

Overview

A prospective evaluation of postoperative corneal aberrations and visual parameters (e.g. visual acuity) in patients implanted with an AcrySof Toric IOL.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Conditions

Cataracts Astigmatism

Interventions

ToricDEVICE

AcrySof Toric IOL

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Operable cataracts; * Good ocular health; * Qualifies for AcrySof Toric IOL via AcrySof Toric Calculator (1.03-2.06 D cylinder at corneal plane) Exclusion Criteria: * \>2.06 D astigmatism at corneal plane; * irregular astigmatism; * prior or ongoing corneal disease or scarring; * history of ocular disease

Outcomes

Primary Outcomes

Corneal Aberration

Time frame: 3 months

Secondary Outcomes

Visual acuity, residual refractive cylinder, lens alignment

Time frame: 3 months

Data from ClinicalTrials.gov

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