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

NCT ID: NCT00878839

Last Updated: 2012-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2009-03-31

Study Completion Date

2009-03-31

Brief Summary

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

Detailed Description

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Conditions

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Cataracts Astigmatism

Keywords

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Cataract Toric IOL Corneal Aberration Astigmatism AcrySof

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Toric

AcrySof Toric IOL to assess corneal aberration

Group Type OTHER

Toric

Intervention Type DEVICE

AcrySof Toric IOL

Interventions

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Toric

AcrySof Toric IOL

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Alcon Research

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Countries

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Mexico

Other Identifiers

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M09-016

Identifier Type: -

Identifier Source: org_study_id