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Surgical Reduction of the Inferior Turbinates for Nasal Obstruction

NCT00737906 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-08-26

No results posted yet for this study

Summary

The primary goal of this post-marketing surveillance study is to assess whether surgical turbinate reduction performed using a Coblation® device is associated with reduced nasal obstruction symptoms.

Conditions

  • Chronic Rhinitis
  • Inflammation of the Nasal Mucosa
  • Inflammation of Nasal Tissue

Interventions

PROCEDURE

Surgical turbinate reduction procedure

Surgical turbinate reduction using the COBLATION device

Sponsors & Collaborators

  • ArthroCare Corporation

    lead OTHER

Principal Investigators

  • Anthony M Magit, MD · Children's Associated Medical Group, San Diego, CA

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00737906 on ClinicalTrials.gov