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Clinical Trial Summary

The objective of this study is to evaluate the efficacy of PROPEL Contour placement following an in-office frontal sinus balloon dilation (SBD) in patients with chronic rhinosinusitis (CRS)


Clinical Trial Description

A post-market, randomized, intra-patient controlled, blinded multicenter study with 80 randomized subjects at up to 20 study centers. After successful in-office bilateral balloon dilation of the frontal sinus ostium (FSO) using the VenSureā„¢ Nav Balloon Device and Fiagon Cube Navigation System, patients will be randomized to receive one PROPEL Contour Sinus Implant on one side while the contralateral side serves as the control. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04858802
Study type Interventional
Source Intersect ENT
Contact
Status Completed
Phase N/A
Start date May 12, 2021
Completion date June 20, 2022

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