Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients

Alcon Research

Overview

A prospective evaluation of postoperative corneal aberrations and visual parameters in patients assigned to either an AcrySof IQ Toric intraocular lens (IOL) group or a group implanted with a SN60WF IOL and having concomitant limbal relaxing incision.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Conditions

Cataracts

Interventions

ToricDEVICE

Unilateral implantation of the AcrySof IQ Toric IOL

Limbal Relaxing IncisionPROCEDURE

Unilateral implantation of a AcrySof IQ (SN60WF) IOL with concomitant LRI at the time of surgery

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. operable cataracts 2. good ocular health 3. 0.5 D to 2.0 D of corneal astigmatism Exclusion Criteria: 1. \> 2.0 D astigmatism 2. irregular astigmatism 3. prior or ongoing corneal disease or scarring 4. history of ocular disease

Locations (1)

Alcon Call Center for Trial Locations

Fort Worth, Texas, United States

Outcomes

Primary Outcomes

Corneal aberration

Time frame: 3 months

Secondary Outcomes

Visual acuity

Time frame: 3 months

Data from ClinicalTrials.gov

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