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Sinus Balloon Dilation in Pediatric Patients

Sinusitis Clinical Trial

Official title:
XprESS Device and PathAssist Confirmation Tools in Pediatric Patients-Expanded Indication Study

Clinical Trial Summary

Safety and effectiveness of sinus balloon dilation in patients 2-21 years old.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02278484
Study type Interventional
Source Entellus Medical, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date September 2014
Completion date January 2016
View Details
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