Expired Study
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Fort Worth, Texas 76134


Purpose:

The objective of this study is to evaluate postoperative visual function in patients implanted bilaterally with the ReSTOR Aspheric Intraocular Lens (IOL).


Criteria:

Inclusion Criteria: - Bilateral cataract patients who require natural crystalline lens removal and bilateral Intraocular Lens (IOL) implantation. - 50~75 years of age - <1 Diopter of astigmatism preoperatively (before surgery) as measured by Keratometry readings. Exclusion Criteria: - Patients with pre-existing conditions that could skew the results. - Any of conditions before and during surgery specified in the product information.


NCT ID:

NCT00818116


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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