Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4
Completed
- Conditions
- Cataract
- Registration Number
- NCT01215045
- Lead Sponsor
- Alcon Research
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 17
Inclusion Criteria
- Diagnosed with cataracts
Exclusion Criteria
- Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Acuity 6 months
- Secondary Outcome Measures
Name Time Method Contrast sensitivity, patient survey 6 months
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the clinical visual outcomes of bilateral AcrySof ReSTOR Aspheric IOL implantation in cataract patients?
How does the AcrySof ReSTOR Aspheric IOL compare to standard monofocal lenses in terms of spectacle independence?
What biomarkers correlate with improved visual acuity following AcrySof ReSTOR IOL implantation in cataract surgery?
What adverse events are associated with AcrySof ReSTOR Aspheric IOLs in bilateral cataract procedures?
How do aspheric intraocular lenses like AcrySof ReSTOR influence higher-order aberrations in post-cataract eyes?
Trial Locations
- Locations (1)
Contact Alcon Call Center for Trial Locations
🇺🇸Fort Worth, Texas, United States
Contact Alcon Call Center for Trial Locations🇺🇸Fort Worth, Texas, United States