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VivAer: A Correlation Between Symptom Scores and Objective Findings

Airway Obstruction Clinical Trial

Official title:
VivAer: A Correlation Between Symptom Scores and Objective Findings

Clinical Trial Summary

This is a prospective, single-center study. This study seeks to determine the objective improvement in nasal airflow in patients after undergoing the VivAer procedure, which involves the use of a stylus to deliver controlled and targeted low energy radiofrequency heating (heating by applying high-frequency radio waves) to the nasal sidewall to gently reshape the tissues. Patients who experience refractory, or medically unexplained, nasal obstruction often have symptoms that are not alleviated or resolved by standard non-surgical treatment options. VivAer, a recently developed, FDA-approved procedure, is one of the standard surgical treatments for nasal obstruction. Unlike most of the other established surgical treatments for nasal obstruction, however, VivAer is a minimally-invasive procedure, and it is an outpatient intervention that can be performed under local anesthetic. Eligible patients who are enrolled in the study will undergo the VivAer procedure, and will return to the clinic for three in-office follow-up visits at 4, 12, and 24 weeks after the procedure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05573919
Study type Interventional
Source NorthShore University HealthSystem
Contact Riley J Medenwald, BS
Phone 874-570-3944
Email RMedenwald@northshore.org
Status Recruiting
Phase N/A
Start date October 7, 2022
Completion date October 2024
View Details
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