Overview

Nasospore Stent For Use in Enodscopic Sinus Surgery

Status:
Withdrawn
Trial end date:
2012-02-01
Target enrollment:
0
Participant gender:
All
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.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Lahey Clinic
Treatments:
Bacitracin
Gentamicins
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)