Actively Recruiting

Age: 18Years +
All Genders
NCT02038166

Nasal Potential Difference (NPD) Protocol in Chronic Rhinosinusitis

Led by University of Alabama at Birmingham · Updated on 2026-03-17

20

Participants Needed

1

Research Sites

673 weeks

Total Duration

On this page

Sponsors

U

University of Alabama at Birmingham

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to determine if acquired (partial) Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) deficiency contributes substantially to the pathogenic mechanisms underlying Chronic Rhinosinusitis (CRS), creating a localized environment that impairs mucociliary clearance (MCC).

CONDITIONS

Official Title

Nasal Potential Difference (NPD) Protocol in Chronic Rhinosinusitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of chronic rhinosinusitis (CRS) based on Sinus and Allergy Health Partnership criteria with symptoms lasting 12 weeks or more
  • Presence of signs of nasal inflammation such as discolored nasal drainage, nasal polyps, middle meatus or ethmoid bulla swelling, or confirmed mucosal changes on CT scan
  • Age 19 years or older
  • Weight at least 50 kilograms
  • Ability to perform Nasal Potential Difference (NPD) testing
  • Negative pregnancy test for females of childbearing potential
  • Provide written informed consent
Not Eligible

You will not qualify if you...

  • Acute illness within 2 weeks before starting study procedures
  • Major asthma attack within 2 months prior to study
  • Change in intranasal medications within 14 days before study
  • Positive test for hepatitis B, hepatitis C, or HIV
  • Hemoglobin less than 10 gm/dL or serum albumin less than 2.5 g/dL
  • Abnormal liver function tests above twice the normal range
  • Abnormal kidney function with serum creatinine above 1.5 times normal
  • Pregnancy or breastfeeding
  • History of solid organ or blood cell transplantation
  • History of autoimmune or granulomatous disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35244

Actively Recruiting

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Research Team

N

Norma Miller, RN

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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