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Safety and Effectiveness of the Calhoun Vision Light Adjustable Intraocular Lens (LAL)

Cataracts Clinical Trial

Official title:
A Prospective Multi-center Clinical Study to Evaluate the Safety and Effectiveness of the Light Adjustable Lens (LAL) in Subjects Undergoing Cataract Extraction

Clinical Trial Summary

The primary objective of this study is to evaluate, for the visual correction of aphakia, the safety and effectiveness of the Calhoun Vision Light Adjustable intraocular lens (LAL) and Light Delivery Device (LDD) in treating postoperative residual refractive error by providing a stable, targeted refractive adjustment of the LAL power and lock-in treatments with the LDD.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00845520
Study type Interventional
Source Calhoun Vision, Inc.
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date March 2013
View Details
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