Nasospore Stent For Use in Enodscopic Sinus Surgery

Status Withdrawn

Clinical Trial Summary

The purpose of this study is to evaluate a stenting material called Nasopore. This is a synthetic material approved by FDA for use as a stent in postoperative sinus surgery patients. This study will compare the Nasopore stent to other approved stenting materials.

Clinical Trial Description

This study will compare other sinus stenting products to the Nasopore stent. The stents will be soaked in antibiotic solutions and be observed for how well they perform. Subjects will have a stent placed in each sinus, stents may be the standard antibiotic saturated materials or the new nasopore material or nasopore stent soaked in antibiotics. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Chronic Sinusitis

Clinical Trial Details

NCT number	NCT00671541
Study type	Interventional
Source	Lahey Clinic
Contact
Status	Withdrawn
Phase	Phase 4
Start date	March 2006
Completion date	February 2012

View Details

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