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Clinical Trial Summary

This study aims to compare the clinical performance and subjective acceptance of the comfilcon A and the omafilcon B soft contact lenses.

Clinical Trial Description

This will be a randomized, subject-masked, crossover, bilateral study, controlled by cross comparison. Thirty subjects will use each lens type for two weeks in random sequence. Follow-up visits for each lens will be performed after two weeks of wear. Lenses will be worn on a daily wear basis.

The final optical design of comfilcon A contact lens was optimized to improve the quality and two further studies (CV-18-10 and CV-18-11) were conducted after completion of this study to evaluate the modified optical design. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT03006458
Study type Interventional
Source Coopervision, Inc.
Status Completed
Phase N/A
Start date December 2016
Completion date April 6, 2017

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