FinESS Registry Study

Entellus Medical

Status: Completed

Conditions: Rhinosinusitis

Study type: Observational

Funder types: Industry

Identifiers

NCT00849953

1498-001

Details and patient eligibility

About

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.

Enrollment: 500 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

500 participants in 1 patient group

FinESS Treatment

Description:

Subjects undergoing treatment with the FinESS Sinus Treatment System