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Clinical Trials/NCT01553110
NCT01553110
Completed
Not Applicable

An Observational Study to Evaluate The Relationship of Nasal Mucus Properties and Symptoms in Acute Rhinosinusitis.

Virginia Commonwealth University1 site in 1 country41 target enrollmentMarch 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Rhinosinusitis
Sponsor
Virginia Commonwealth University
Enrollment
41
Locations
1
Primary Endpoint
Nasal Secretion Collection
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This is a study to learn more about the common cold from studying the nasal secretions produced during a cold or episode of allergic rhinitis.

Detailed Description

This study involves collecting and analyzing nasal mucus to see if there are changes in mucus properties during the course of a cold or episode of allergic rhinitis. Outcome measures include SNOT20 questionnaire, nasal secretion collection, acoustic rhinometry on the fifth and fourteenth day of symptoms. The investigators will also collect SNOT20 questionnaires on the tenth and twenty-eighth day.

Registry
clinicaltrials.gov
Start Date
March 2012
End Date
April 2019
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male and female subjects 12 years of age and older with acute nasal discharge fewer than 7 days or a history suggesting nasal allergic symptoms for at least 1 year. Internet access required during the course of the study. Patients must be symptomatic at screening.

Exclusion Criteria

  • Symptoms suggesting bacterial rhinosinusitis such as fever ≥ 101ºF/38.3ºC, facial swelling, and serve tooth pain. History of CRS or sinus/nasal surgery for this condition within 6 months before screening. History of respiratory signs and symptoms due to allergic rhinitis. Therapy with bronchodilators, nasal steroids, oral corticosteroids in the past 30 days. Therapy with antihistamines, nasal (Neti) washings, or decongestants in the past 24 hours. Use of any OTC cold or allergy medication 24 hours before study visits requires a 24 hour washout phase

Outcomes

Primary Outcomes

Nasal Secretion Collection

Time Frame: 10 minutes

To measure the biophysical properties of nasal secretions for improved mucus clearance.

Secondary Outcomes

  • Subjective nasal scoring(10 Minutes)
  • Nasal Volume(15 Minutes)

Study Sites (1)

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