Expired Study
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Burlington, Massachusetts 01805


Purpose:

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.


Study summary:

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.


Criteria:

Inclusion Criteria: - Evaluation by Otolaryngologist & determined to need endoscopic sinus surgery - Only subjects with Bilateral disease Exclusion Criteria: - Pediatric subjects(under the age of 18)


NCT ID:

NCT00671541


Primary Contact:

Principal Investigator
Peter J. Catalano, MD
Lahey Clinic


Backup Contact:

N/A


Location Contact:

Burlington, Massachusetts 01805
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 22, 2018

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