Using Navigation to Improve Accuracy of Maxillary Balloon Sinusotomy

PHASE2/PHASE3RecruitingINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

September 4, 2024

Primary Completion Date

October 1, 2025

Study Completion Date

December 31, 2025

Conditions
Chronic Maxillary Rhinosinusitis
Interventions
DEVICE

RELIEVA SPINPLUS® NAV Balloon Sinusplasty System

The non-navigated device being used is the RELIEVA SPINPLUS® Balloon Sinusplasty System and the navigated device being used is the RELIEVA SPINPLUS® NAV Balloon Sinusplasty System. Both devices being used are standard devices that are currently FDA approved and used in practice for sinus dilation at Cedars-Sinai Medical Center.

Trial Locations (1)

90048

RECRUITING

Cedars Sinai, Los Angeles

All Listed Sponsors
lead

Cedars-Sinai Medical Center

OTHER