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LATERA-OFFICE Study

Nasal Obstruction Clinical Trial

Official title:
Spirox Latera™ Implant Support of Lateral Nasal Wall Cartilage (LATERAL-OFFICE) Study

Clinical Trial Summary

Prospective, multicenter, nonrandomized, single-arm controlled study to obtain outcomes data in participants with severe to extreme class NOSE scores who are undergoing placement of the Spirox Latera Implant with or without concurrent turbinate reduction procedures in an office setting.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02964312
Study type Interventional
Source Spirox, Inc.
Contact
Status Completed
Phase N/A
Start date November 10, 2016
Completion date August 29, 2019
View Details
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