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Clinical Trials/NCT00878839
NCT00878839WithdrawnNot Applicable

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

Alcon Research0 sitesStarted: March 2009Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Primary Endpoint
Corneal Aberration
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

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