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Clinical Trial Summary

The primary objective of thes study is to confirm that the ocular response to the Test lenses are similar to those of the Control lenses when used in a 1 week planned replacement, daily wear modality over a 1-month period.


Clinical Trial Description

The test lens and control lens were randomized in a 2:1 ratio to evaluate the test lens and control contact lens. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01706770
Study type Interventional
Source Coopervision, Inc.
Contact
Status Completed
Phase N/A
Start date May 2012
Completion date October 2012

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