XprESS Registry Study

NACompletedINTERVENTIONAL
Enrollment

175

Participants

Timeline

Start Date

April 30, 2010

Primary Completion Date

December 31, 2011

Study Completion Date

December 31, 2011

Conditions
Sinusitis
Interventions
DEVICE

XprESS Balloon Device

Sinus dilation completed with the XprESS Balloon Device with or without additional endoscopic sinus surgery procedures (dilation of the frontal recesses, maxillary ostia, and/or sphenoid sinus ostia).

Trial Locations (1)

78006

Texas Sinus Center, San Antonio

Sponsors
All Listed Sponsors
lead

Entellus Medical, Inc.

INDUSTRY

NCT01115309 - XprESS Registry Study | Biotech Hunter | Biotech Hunter