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Clinical Trials/NCT00721253
NCT00721253
Completed
Phase 4

Visual Outcomes of Subjects Bilaterally Implanted With ReSTOR Aspheric +4 vs. Tecnis Multifocal Intraocular Lens (IOL) or Acri.LISA IOL

Alcon Research1 site in 1 country42 target enrollmentJuly 2007
ConditionsCataract

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Cataract
Sponsor
Alcon Research
Enrollment
42
Locations
1
Primary Endpoint
Uncorrected Visual Acuity (UCVA) at Distance, Near and Intermediate
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

This is a study to compare visual outcomes of subjects bilaterally implanted w/ReSTOR to subjects bilaterally implanted with the Tecnis Multifocal Intraocular Lens (IOL) or Acri.LISA IOL

Registry
clinicaltrials.gov
Start Date
July 2007
End Date
October 2008
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with cataracts

Exclusion Criteria

  • Preexisting condition likely to confound results; 1 D astigmatism by preoperative K-readings

Outcomes

Primary Outcomes

Uncorrected Visual Acuity (UCVA) at Distance, Near and Intermediate

Time Frame: 6 months

Uncorrected Visual Acuity (UCVA) at distance, near and intermediate, measured in logMAR. LogMAR is the "logarithm of the minimum angle of resolution". It is a unit of measure for visual acuity (VA). A lower logMAR value indicates better visual acuity.

Secondary Outcomes

  • Contrast Sensitivity(6 months)
  • Defocus Curve(6 months post-operative)

Study Sites (1)

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