Status:
COMPLETED
Rotational Stability of the AcrySof® Toric
Lead Sponsor:
Alcon Research
Conditions:
Cataract
Eligibility:
All Genders
40-80 years
Phase:
NA
Brief Summary
To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.
Eligibility Criteria
Inclusion
- Monolateral or bilateral cataracts
- anticipated intraocular lens (IOL) power of +10 Diopters (D) \~ +25D
- 75 \~ 2.0 D of astigmatism measured preoperatively by Keratometry readings
- able to sign the informed consent, to comply with scheduled visits and other study procedures
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
- uncontrolled diabetes
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
71 Patients enrolled
Trial Details
Trial ID
NCT00762216
Start Date
May 1 2008
Last Update
October 31 2012
Active Locations (1)
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1
Alcon Call Center
Fort Worth, Texas, United States, 76134