NCT01214863CompletedNot Applicable
Clinical Results With the AcrySof Toric Intraocular Lens (IOL)
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Alcon Research
- Enrollment
- 144
- Locations
- 1
- Primary Endpoint
- Visual Acuity
Study Overview
Brief Summary
This study is an evaluation of visual outcomes of subjects implanted with the AcrySof Toric Intraocular Lenses (IOLs) Models SN60T3, SN60T4, and SN60T5.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Diagnosed with cataracts; has astigmatism falling in range of AcrySof Toric lens as assessed by the AcrySof Toric calculator
Exclusion Criteria
- •Ocular comorbidities affecting visual outcome data,
- •Prior refractive surgery,
- •Irregular astigmatism
Outcomes
Primary Outcomes
Visual Acuity
Time Frame: 1 day to 6 months
Secondary Outcomes
- Postoperative refractive cylinder(1day to 6 months)
Investigators
Study Sites (1)
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