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Clinical Trial Summary

This study is being conducted to obtain outcomes data in subjects with severe to extreme class NOSE scores undergoing placement of the Spirox Latera Implant with or without concurrent septoplasty and/or turbinate reduction procedures in an operating room setting.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02952313
Study type Interventional
Source Spirox, Inc.
Contact
Status Completed
Phase N/A
Start date September 2016
Completion date August 2019

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