MedPath

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

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
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (14)

Gulf Coast Facial Plastics and ENR

🇺🇸

Panama City, Florida, United States

South Denver ENT and Allergy

🇺🇸

Denver, Colorado, United States

Gensys Regional Medical Center

🇺🇸

Grand Blanc, Michigan, United States

Paparella Group

🇺🇸

Maple Grove, Minnesota, United States

Lee's Summit Ear, Nose and Throat Center

🇺🇸

Lee's Summit, Missouri, United States

Dickson Ear, Nose and Throat PLC

🇺🇸

Dickson, Tennessee, United States

Midwest Ear, Nose and Throat

🇺🇸

Sioux Falls, South Dakota, United States

St. Cloud Ear Nose and Throat

🇺🇸

St Cloud, Minnesota, United States

Medical Center ENT Associates of Houston

🇺🇸

Houston, Texas, United States

Austin Ear, Nose and Throat Clinic

🇺🇸

Austin, Texas, United States

Capital Otolaryngology

🇺🇸

Austin, Texas, United States

Texas Sinus Center

🇺🇸

Boerne, Texas, United States

Advanced Ear, Nose and Throat Specialists

🇺🇸

Milwaukee, Wisconsin, United States

Advanced Otolaryngology, PC

🇺🇸

Richmond, Virginia, United States

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