Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3
Phase 4
Completed
- Conditions
- Cataract
- Interventions
- Device: ReSTOR
- Registration Number
- NCT00719732
- Lead Sponsor
- Alcon Research
- Brief Summary
A prospective evaluation of the visual parameters in a series of patients bilaterally implanted with AcrySof ReSTOR +3 Intraocular Lens (IOL).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 218
Inclusion Criteria
- Diagnosed with cataracts
Exclusion Criteria
- Pre-existing conditions that could skew the results or are contraindications for the ReSTOR intraocular lens;
- <1 diopter astigmatism by keratometry readings.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description ReSTOR Aspheric +3 ReSTOR Enrolled subjects receive implantation of ReSTOR +3 intraocular lenses (IOLs) for replacement of cataract in the natural lens of the eye. The patients were to be implanted bilaterally (in both eyes).
- Primary Outcome Measures
Name Time Method Uncorrected Visual Acuity (UCVA) 6 months Uncorrected Visual Acuity (UCVA) measured by means of logMAR at various distances (40 centimeters (cm), 50 cm, 60 cm, 70 cm, and 4 meters (m)). Visual Acuity (VA) is measured in logMAR. LogMAR is the "logarithm of the minimum angle of resolution". A lower logMAR value indicates better visual acuity.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Alcon Call Center for Trial Locations
🇺🇸Fort Worth, Texas, United States