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SinuSys Patency of Frontal Recess and Sphenoid Sinus Ostia Study

Sinusitis Clinical Trial

Official title:
SinuSys Patency of Frontal Recess and Sphenoid Sinus Ostia Study

Clinical Trial Summary

The goal of this study is to evaluate basic usability and confirm expected safety and effectiveness of SinuSys Dilation System when used to dilate frontal recess and sphenoid sinus ostia in patients with chronic rhinosinusitis.

Clinical Trial Description

A multicenter, single arm, prospective study conducted to assess the safety and effectiveness of an osmotically-drive, low-pressure expansion device for dilation of frontal recess and sphenoid sinus ostia in patients with chronic rhinosinusitis (CRS). ;

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 NCT02463279
Study type Interventional
Source SinuSys Corporation
Contact
Status Completed
Phase N/A
Start date April 2015
Completion date March 2016
View Details
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