Status:
COMPLETED
Visual Function After Bilateral Implantation of AcrySof® Toric
Lead Sponsor:
Alcon Research
Conditions:
Visual Function
Eligibility:
All Genders
40-80 years
Phase:
PHASE4
Brief Summary
The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.
Eligibility Criteria
Inclusion
- Bilateral cataracts
- 40\~80 years of age
- 4 Days - 1 Week interval between a single patient's surgery
- dilated pupil size (in dim light) ≥ 4.0 mm
- Anticipated correction with an IOL of +10 Diopters \~ +25 Diopters
- 75 - 2.0 Diopters of astigmatism preoperatively as measured by Keratometry readings
Exclusion
- Preoperative ocular pathology
- Previous intraocular or corneal surgery
- An increased risk for complications which could require vitreoretinal surgery
- Corneal irregularities
- Corneal opacities
- Current contact lens usage(within 6 months prior to first surgery)
Key Trial Info
Start Date :
April 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT00758550
Start Date
April 1 2007
Last Update
March 16 2010
Active Locations (1)
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1
Alcon Call Center
Fort Worth, Texas, United States, 76134