Status:
WITHDRAWN
Recommendations for Monitoring Clinical Experience Following Implantation of the AcrySof® Toric
Lead Sponsor:
Alcon Research
Conditions:
Cataract
Eligibility:
All Genders
40-80 years
Phase:
PHASE4
Brief Summary
To allow surgeons to obtain clinical experience on the postoperative uncorrected and best distance corrected visual acuities (UCVA and BDCVA) and corneal and refractive cylinder of the AcrySof Toric I...
Eligibility Criteria
Inclusion
- 40-80 years old; of any race and gender; diagnosed with bilateral cataracts; require cataract extraction followed by implantation of a posterior chamber IOL; patients have between 0.75 -2.5 D of astigmatism preoperatively as measured by K readings.
Exclusion
- Females of child bearing potential;irregular corneal astigmatism;keratopathy/Keratectasia; cornea inflammation or edema;previous corneal reshaping,dystrophy or transplant;amblyopia;glaucoma;RPE/Macular changes;diabetic retinopathy.
Key Trial Info
Start Date :
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00761488
Last Update
May 12 2015
Active Locations (1)
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1
Alcon Call Center
Fort Worth, Texas, United States, 76134