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Clinical Trials/NCT00878839
NCT00878839
Withdrawn
Not Applicable

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

Alcon Research0 sitesMarch 2009
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ConditionsCataractsAstigmatism

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataracts
Sponsor
Alcon Research
Primary Endpoint
Corneal Aberration
Status
Withdrawn
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
March 2009
End Date
March 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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(3 months)

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