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