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Clinical Trial Summary

The primary study objectives are: to evaluate (1) the change in ocular discomfort at 30 days and (2) the change in signs and symptoms of ocular surface disease in demodex-positive subjects beginning the use of Avenova.


Clinical Trial Description

This is a prospective study of subjects who have been diagnosed with bilateral demodex blepharitis. Qualified symptomatic eyes will be randomized and monitored for 30 days; one eye will undergo Avenova treatment twice daily and one eye will not undergo any study treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02938078
Study type Interventional
Source Minnesota Eye Consultants, P.A.
Contact
Status Terminated
Phase N/A
Start date October 2016
Completion date August 24, 2018

See also
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