Status:
WITHDRAWN
Nasospore Stent For Use in Enodscopic Sinus Surgery
Lead Sponsor:
Lahey Clinic
Conditions:
Chronic Sinusitis
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief 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 c...
Detailed 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 pla...
Eligibility Criteria
Inclusion
- Evaluation by Otolaryngologist \& determined to need endoscopic sinus surgery
- Only subjects with Bilateral disease
Exclusion
- Pediatric subjects(under the age of 18)
Key Trial Info
Start Date :
March 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00671541
Start Date
March 1 2006
End Date
February 1 2012
Last Update
February 17 2012
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Lahey Clinic, Inc
Burlington, Massachusetts, United States, 01805