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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 NCT04525170
Study type Interventional
Source Contamac Ltd
Contact
Status Withdrawn
Phase N/A
Start date September 2015
Completion date December 2015

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