FinESS Registry Study

Completed

• Conditions: Rhinosinusitis

• Registration Number: NCT00849953
• Lead Sponsor: Entellus Medical, Inc.

Brief Summary

A prospective, post-approval registry study assessing subject rhinosinusitis symptomatic status over time following treatment with FinESS Sinus Treatment using self-administered quality of life survey data.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2009-02-20
• Study First Submitted QC: 2009-02-20
• Study First Posted: 2009-02-24
• Study Start: 2009-03
• Primary Completion: 2011-03
• Study Completion: 2011-03
• Status Verified: 2011-06
• Last Update Submitted: 2011-06-27
• Last Update Posted: 2011-06-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 500

Inclusion Criteria

• adults 18 years or older undergoing balloon dilation with FinESS Sinus Treatment and have provided voluntary consent to participate in Registry

Exclusion Criteria

• none

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (14)

South Denver ENT and Allergy; 🇺🇸 Denver, Colorado, United States

Gulf Coast Facial Plastics and ENR; 🇺🇸 Panama City, Florida, United States

Gensys Regional Medical Center; 🇺🇸 Grand Blanc, Michigan, United States

Paparella Group; 🇺🇸 Maple Grove, Minnesota, United States

St. Cloud Ear Nose and Throat; 🇺🇸 St Cloud, Minnesota, United States

Lee's Summit Ear, Nose and Throat Center; 🇺🇸 Lee's Summit, Missouri, United States

Midwest Ear, Nose and Throat; 🇺🇸 Sioux Falls, South Dakota, United States

Dickson Ear, Nose and Throat PLC; 🇺🇸 Dickson, Tennessee, United States

Austin Ear, Nose and Throat Clinic; 🇺🇸 Austin, Texas, United States

Capital Otolaryngology; 🇺🇸 Austin, Texas, United States

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