Expired Study
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Fort Worth, Texas 76134


Purpose:

To collect visual outcome data post AcrySof ReSTOR Aspheric +4 implantation from surgeons throughout the United States.


Criteria:

Inclusion Criteria: - operable cataracts; candidate for presbyopic correcting intraocular lens (IOL) Exclusion Criteria: - ocular comorbidities confounding study outcomes


NCT ID:

NCT00733512


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 21, 2018

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