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Clinical Trial Summary

Study to assess the safety and efficacy of the XprESS device for transnasal Eustachian tube dilation.


Clinical Trial Description

Prospective, multicenter, randomized controlled trial comparing balloon dilation of the Eustachian tube to continued medical management for treatment of persistent Eustachian tube dysfunction. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02391584
Study type Interventional
Source Entellus Medical, Inc.
Contact
Status Completed
Phase N/A
Start date February 2015
Completion date October 2017

See also
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