FinESS Registry Study

Completed

Conditions studied: Rhinosinusitis

In brief

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.

Key facts

Study ID

NCT00849953

Run by

Entellus Medical, Inc.

People needed

500

Starts

2009-03-01

Expected to finish

2011-03-01

Last updated by the study team

2011-06-28

Who can join

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

You may qualify if…

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

You may not qualify if…

• none

Where it is running

• 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 — Saint 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
• Texas Sinus Center — Boerne, Texas, United States
• Medical Center ENT Associates of Houston — Houston, Texas, United States
• Advanced Otolaryngology, PC — Richmond, Virginia, United States
• Advanced Ear, Nose and Throat Specialists — Milwaukee, Wisconsin, United States

Full record on ClinicalTrials.gov

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