Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide

NACompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

November 30, 2011

Study Completion Date

November 30, 2011

Conditions
Sinusitis
Interventions
DEVICE

Stratus Microflow Ethmoid Spacer

The Spacer is inserted surgically into the ethmoid complex through the use of a sinus access system. Triamcinolone acetonide will be administered into the Spacer for this investigational study. The Spacer will be left in the ethmoid sinus for a period of 28 days. At the end of the implant period, the device is removed with standard instrumentation, during a follow-up office visit.

Trial Locations (1)

01805

Lahey Clinic, Burlington

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Acclarent

INDUSTRY

lead

Integra LifeSciences Corporation

INDUSTRY

NCT00791934 - Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide | Biotech Hunter | Biotech Hunter