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

Sinusitis Clinical Trial

Official title:
Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide (Kenalog-40)

Clinical Trial Summary

Study Design:

A non-randomized, multi-center, prospective, clinical study intended to evaluate the safety and efficacy of treating the ethmoid sinuses with the Ethmoid Sinus Spacer and Access System used for the local delivery of Triamcinolone Acetonide, over a period of 28 days.

Clinical Trial Description

n/a

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 NCT00791934
Study type Interventional
Source Acclarent
Contact
Status Completed
Phase Phase 3
Start date August 2008
Completion date November 2011
View Details
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