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Visual Function Evaluation of Bilateral AcrySof ReSTOR Aspheric IOL

Cataracts Clinical Trial

Official title:
Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric Intraocular Lens (IOL): Postmarket Evaluation

Clinical Trial Summary

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

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00818116
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase Phase 4
Start date December 2008
View Details
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