Nasospore Stent For Use in Enodscopic Sinus Surgery

Withdrawn before enrolling · Phase 4

Conditions studied: Chronic Sinusitis

In brief

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.

Key facts

Study ID

NCT00671541

Run by

Lahey Clinic

People needed

0

Starts

2006-03-01

Expected to finish

2012-02-01

Last updated by the study team

2012-02-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Evaluation by Otolaryngologist \& determined to need endoscopic sinus surgery
• Only subjects with Bilateral disease

You may not qualify if…

• Pediatric subjects(under the age of 18)

Where it is running

• Lahey Clinic, Inc — Burlington, Massachusetts, United States

Full record on ClinicalTrials.gov

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