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Safety and Performance of the SinuSys Dilation System for Dilation of the Maxillary Sinus Ostium

Sinusitis Clinical Trial

Official title:
SinuSys Patency of Maxillary Sinus Ostia Study

Clinical Trial Summary

The purpose of this study is to assess safety and performance of the SinuSys Dilation System for dilation of the maxillary sinus ostium.

Clinical Trial Description

A multicenter, single-arm, prospective study conducted to assess the safety and effectiveness of a new osmotically-driven, low-pressure expansion device for dilation of maxillary sinus ostia in patients with (CRS) Chronic Rhinosinusitis ;

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 NCT01623050
Study type Interventional
Source SinuSys Corporation
Contact
Status Completed
Phase Phase 1
Start date April 2012
Completion date September 2014
View Details
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