Expired Study
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Fort Worth, Texas 76134


Purpose:

A prospective evaluation of the visual parameters in a series of patients bilaterally implanted with AcrySof ReSTOR +3 Intraocular Lens (IOL).


Criteria:

Inclusion Criteria: - Diagnosed with cataracts Exclusion Criteria: - Pre-existing conditions that could skew the results or are contraindications for the ReSTOR intraocular lens; - <1 diopter astigmatism by keratometry readings.


NCT ID:

NCT00719732


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: January 20, 2018

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