Measuring Nasal Airway Changes After VivAer Treatment Using AI Analysis

NCT07574918 · tracked via the Priya Life Science USA tracker

Sponsor

Aerin Medical

Phase

Not applicable

Started

2026-11

Last updated

2026-10-30

Condition(s) studied

Nasal Airway Obstruction

Investigational drug(s) / intervention(s)

VivAer Stylus

VivAer Stylus: Bipolar radiofrequency energy delivered to the lateral nasal wall at the upper lateral cartilage using the VivAer® Stylus and Aerin Console at device default settings (temperature 60°C, power 4 watts, treatment time 18 seconds, cooling time 12 seconds) to remodel submucosal tissue, including cartilage, in the internal nasal valve area.

Study summary

The goal of this clinical trial is to measure changes in the nasal airway after treatment with the VivAer® procedure in adults aged 22 to 85 with nasal airway obstruction caused by nasal valve dysfunction. The main questions it aims to answer are:

Are there measurable changes in the nasal airway and airflow after treatment with the VivAer procedure?

Participants will:

Undergo the VivAer procedure, which uses radiofrequency energy to remodel tissue in the nasal valve area. Have endoscopic images of their nasal airway taken before treatment and at follow-up visits at 3 and 6 months after treatment, which will be analyzed using the VISIONAIR™ AI System. They will complete symptom and quality of life surveys at each visit, including the Nasal Obstruction Symptom Evaluation (NOSE) Scale, the STOP-BANG Sleep Score, and the Short-Form (SF-12) Health Survey.

Eligibility

Sex

ALL

Min age

22 Years

Max age

85 Years

Healthy volunteers

Inclusion Criteria: 1. Age 22 to 85 years old (inclusively). 2. Willing and able to provide consent. 3. Willing and able to comply with the patient-specific requirements and follow-up schedule outlined in the study protocol. 4. Has a NOSE Score of ≥ 55. 5. Has a documented diagnosis of NAO with NVC (static or dynamic) as the primary driver of NAO symptoms. 6. Has a documented positive Modified Cottle Maneuver (using curette or equivalent to perform maneuver and evaluate nasal valve function). Exclusion Criteria: 1. Has had rhinoplasty, septoplasty, inferior turbinate reduction or functional endoscopic surgery (FESS) within the preceding 3 months. 2. Has uncontrolled chronic rhinitis as a contributor to nasal obstruction symptoms. 3. Has a complex nasal anatomy (e.g., anatomical deformity) or a history of significant nasal trauma that is a potential contributor to nasal obstruction symptoms. 4. Has any intranasal conditions that preclude adequate visualization of the nasal valve area. 5. Has a medical condition(s) that may impair normal healing processes. 6. Any adjunctive surgical or other nasal procedure (e.g., concha bullosa resection, inferior turbinate out fracture, septoplasty, etc.) on the same day or planned within 6 months of the study procedure. 7. Has current or recent (within 30 days prior to screening) exposure to oral systemic corticosteroids or is expected to require oral corticosteroid therapy during the course of the study. 8. Has nasal polyps, or a history of nasal polyps requiring medical or surgical treatment within the past 12 months.

Primary outcome measure(s)

Change in nasal valve angle and cross-sectional area — Baseline to 3- and 6-months post-procedure.
Quantitatively assess anatomic improvement of the internal nasal valve (INV) and nasal airway following VivAer treatment using VISIONAIR™ analysis.

Trial sites (1)

Facility	City	Region	Status
ENT & Allergy of Delaware	Newark	Delaware	Recruiting

More Aerin Medical trials in the USA

A Study of RhinAer Stylus for Treating Chronic Rhinitis Active, not recruiting

A Prospective Study Comparing VivAer to Alternative Surgical Procedures to Treat Nasal Airway Obstruction in Patients With Nasal Valve Dysfunction. Active, not recruiting

Other trials for the same condition

Open-Label Study to Evaluate the Safety and Effectiveness of the Spirair Implant Active, not recruiting

A Prospective Study Comparing VivAer to Alternative Surgical Procedures to Treat Nasal Airway Obstruction in Patients With Nasal Valve Dysfunction. Active, not recruiting

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07574918 on ClinicalTrials.gov ↗ ← All trials in the USA