NCT01215045CompletedNot Applicable
Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Alcon Research
- Enrollment
- 17
- Locations
- 1
- Primary Endpoint
- Visual Acuity
Study Overview
Brief Summary
Determine the clinical visual outcomes following bilateral implantation of the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) and to demonstrate what percentage of the subjects obtain spectacle freedom.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Diagnosed with cataracts
Exclusion Criteria
- •Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism
Outcomes
Primary Outcomes
Visual Acuity
Time Frame: 6 months
Secondary Outcomes
- Contrast sensitivity, patient survey(6 months)
Investigators
Study Sites (1)
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