Contralateral ReSTOR / Monofocal or Phakic Eye
- Conditions
- Cataracts
- Registration Number
- NCT00731640
- Lead Sponsor
- Alcon Research
- Brief Summary
Bilateral evaluation of unilateral implantation of ReSTOR and contralateral monofocal or phakic eye.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 52
- Unilateral operable cataract
- Candidate for presbyopic intraocular lens (IOL)
- Ocular comorbidities compromising primary outcome
- Bilateral cataracts
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Visual Acuity 6 months Uncorrected 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 Contrast Sensitivity 6 Months Contrast sensitivity is the measurement of one's ability to detect slight changes in luminance before it becomes indistinguishable. It is measured in logarithmic (log) units by means of an illuminated box, the CSV 1000 by Vector Vision. A higher value for the logarithmic units translates to better contrast sensitivity.
Patient Satisfaction 6 Months Postoperative Average rating of patient satisfaction based on a patient survey. The survey had a 10 point scale (10 being most satisfied and 0 being most unsatisfied).
Spectacle Independence 6 Months The percentage of patients reporting spectacle independence (no longer needing to wear glasses).
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.
Trial Locations
- Locations (1)
Alcon Call Center for Trial Locations
🇺🇸Fort Worth, Texas, United States
Alcon Call Center for Trial Locations🇺🇸Fort Worth, Texas, United States