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Clinical Trial Summary

The aim of the study is to evaluate if the performance of Invigor A is substantially equivalent to Invigor B contact lenses when used in a one month recommended replacement, daily wear modality.


Clinical Trial Description

This study is a multi-centered, daily wear, monthly replacement, bilateral, randomized in a ratio of two to one (2:1) Test to Control, lens blocked (subjects remain in the same lens brand throughout the study), licensed investigator and subject masked, concurrent controlled study with a study duration of approximately three months evaluating performance equivalence of Invigor A (test) over Invigor B (control) contact lenses. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03722784
Study type Interventional
Source Coopervision, Inc.
Contact
Status Completed
Phase N/A
Start date October 10, 2018
Completion date June 1, 2019

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