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Clinical Trial Summary

This study evaluates the safety and effectiveness of the Intranasal Tear Neurostimulator applied intranasally (active) compared with the same device applied extranasally (control) relating to symptoms of dry eye exacerbated by the Controlled Adverse Environment model.


Clinical Trial Description

Participants will be randomized to a single application sequence, either sequence "A" (intranasal application followed by control application) or sequence "B" (control application followed by intranasal application) using the device. Upon entering the CAE, participants will complete dry eye questionnaires every five minutes and will administer the device either intranasally or extranasally in randomized sequence when a certain level of ocular discomfort has been reached. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02910713
Study type Interventional
Source Allergan
Contact
Status Completed
Phase N/A
Start date September 30, 2016
Completion date October 31, 2016

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