Expired Study
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Fort Worth, Texas 76134


Purpose:

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.


Criteria:

Inclusion Criteria: - Monolateral or bilateral cataracts - anticipated intraocular lens (IOL) power of +10 Diopters (D) ~ +25D - 0.75 ~ 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 Criteria: - 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


NCT ID:

NCT00762216


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Fort Worth, Texas 76134
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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