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Clinical Trial Summary

This will be an up to six months, subject-masked, contralateral, parallel-group, randomised, daily wear study. All subjects will wear the Test lens in one eye and the Control lens in the other eye. Data from the first four weeks of Test and Control lens exposure will be used for the FDA 510 (k) submission.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02553681
Study type Interventional
Source Contamac Ltd
Contact
Status Completed
Phase N/A
Start date July 2015
Completion date February 16, 2017

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