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The Nasal Airway in Chronic Obstructive Pulmonary Disease

The Nasal Airway in Chronic Obstructive Pulmonary Disease

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02826954
Acronym
COPD
Enrollment
200
Registered
2016-07-11
Start date
2016-02-29
Completion date
2017-11-30
Last updated
2019-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Keywords

Paranasal Sinus Diseases, Nasal Obstruction

Brief summary

The study is based on the theory of a unified airway that considers the nose and paranasal sinuses together with lower airways as one integrated unit. The upper and lower respiratory tracts function as an interdependent physiologic mechanism, and stimuli that trigger changes in one portion of the airway, can provoke similar changes throughout the airway. This is well documented in asthmatic patients but documented poorly in patients suffering from chronic obstructive lung disease (COPD). COPD is associated with sinonasal symptoms and decreased quality of life. Although nasal involvement has been found to directly affect the lower airway, sinonasal disease is under-diagnosed and under-treated in patients with COPD. This study is embedded in a larger project where the goal is to gain knowledge supporting the theory of a unified airway in patients with COPD. Here sinonasal, pulmonary and generic health related quality of life will be studied in a group of patients with COPD versus a control group. The severity of nasal airway obstruction will be linked to the the severity of pulmonary airway obstruction. Assessment of pathological changes in the nose with nasal endoscopy, as well as performing a nasal cytological brushing for the identification of nasal inflammatory responses in the nose, will be conducted in both the control and study group.

Interventions

OTHERUpper airway assessment, including nasal biopsy

Sponsors

St. Olavs Hospital
CollaboratorOTHER
Haukeland University Hospital
CollaboratorOTHER
University of Copenhagen
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of COPD: all stages * Healthy individuals for the control group

Exclusion criteria

both groups: * asthma * systemic disease such as Cystic Fibrosis, Kartagener syndrome, sarcoidosis * upper airway infection during the last 2 weeks * COPD exacerbation during the last 6 weeks * previous surgery in the nose and paranasal sinuses * ongoing treatment for malignant disease * severe depression, Alzheimers disease and Parkinson's disease * pregnancy or nursing

Design outcomes

Primary

MeasureTime frame
pathological changes in the nose assessed with nasal endoscopy4 hours
inflammatory responses in the nose identified by nasal cytological brushing4 hours

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026