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N/A N=20 Treatment

Treatment Outcome Using Vivaer Stylus to Treat Nasal Airway Obstruction

Nasal Obstruction

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Jun 2021
Primary outcome: Primary: Change in NOSE Score — -44.5 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Vivaer Stylus (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Aerin Medical
Primary completion
Jul 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in NOSE Score
-44.5
PRIMARY
Change in VAS of Nasal Obstruction
-2.6

Summary

This study evaluates subjective and objective measures of treatment outcome after using the Aerin Medical Vivaer™ Stylus to treat nasal obstruction

Eligibility Criteria

Inclusion Criteria

  • Complaints of nasal obstruction for at least 1 year
  • Failed maximum medical therapy (4-6 weeks of steroids)
  • Nasal Obstruction Symptom Evaluation (NOSE) score of ≥ 60 at Baseline
  • Nasal valve is a primary or significant contributor to the subject's nasal obstruction as determined by the study investigator (based on clinical presentation, physical examination, nasal endoscopy, etc.) and the subject has a positive response to any of the following temporary measures (based on patient history or during office exam):
  • Use of external nasal dilator strips (e.g., Breathe Right Strips)
  • Q-Tip test (manual intranasal lateralization)
  • Use of nasal stents
  • Cottle Maneuver (manual lateral retraction of the cheek)

Exclusion Criteria

  • Prior surgical treatment of the nasal valve
  • Rhinoplasty, septoplasty, inferior turbinate reduction or other surgical nasal procedures within the past three (3) months
  • Severe and/or chronic sinusitis, recurrent sinusitis, or allergies leading to nasal obstruction and currently requiring oral corticosteroid therapy
  • Severe case of any of the following: septal deviation, turbinate hypertrophy, polyps, or ptotic nose tip believed to be the primary contributor to the subject's nasal obstruction symptoms and warranting surgical intervention
  • Known or suspected allergies or contraindications to the anesthetic agents and/or antibiotic medications to be used during the study procedure session
  • Known or suspected to be pregnant, or is lactating
  • Other medical conditions which in the opinion of the investigator could predispose the subject to poor wound healing or increased surgical risk
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03156270). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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