Skip to content

The Prevalence of Small Airways Dysfunction In COPD Patients and The Impact on COPD Control

The Prevalence of Small Airways Dysfunction In COPD Patients and The Impact on COPD Control

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04384133
Enrollment
170
Registered
2020-05-12
Start date
2019-10-01
Completion date
2021-04-01
Last updated
2020-05-12

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

Conditions

COPD, Small Airway Disease

Keywords

COPD, Small Airway Dysfunction, Impulse oscillometry

Brief summary

Chronic obstructive pulmonary disease (COPD) is a worldwide prevalent disease. During recent years, increasing attention has been directed to the importance of the contribution of small airways in respiratory diseases. The small airways (usually defined as those with an internal diameter of \<2 mm) are recognized as the major site of resistance to airflow in obstructive lung disease. Although small airway disease is known in chronic airway diseases, the importance of small airway dysfunction on disease control, exacerbations and quality of life, and the importance of taking place among treatable targets is not clear. Therefore, our aim in the study is to determine the frequency of small airway dysfunction in COPD. Our secondary aim is to evaluate the role of small airway dysfunction in disease severity, disease phenotypes, disease control, quality of life and its effect on predicting the risk of exacerbation and its role among treatable targets in chronic airway diseases.

Detailed description

This is a prospective cross-sectional interventional design. 100 COPD patients who applied to Mersin University Faculty of Medicine Hospital Chest Diseases Clinic between 01.10.2019-01.04.2020 will be taken. 35 healthy participants with smoking history and 35 healthy participants without smoking history who were admitted to our clinic within the same date range will be taken as control group. Impulse oscillometric pulmonary function tests will be performed to all participants. Thorax computed tomography will be performed to evaluate small airway dysfunction. To evaluate the degree of disease inflammation and phenotype in COPD patients, nitric oxide measurements will be made in the breath air with fractional exhaled nitric oxide (FENO) device. The blood eosinophil level will be studied to determine the COPD phenotype. To assess symptom control in patients with COPD, mMRC(Modified Medical Research Council) dyspnea scale will be administered. The COPD assessment test (CAT) will be applied to measure the quality of life. All patients will be followed for 1 year to record the number of exacerbations requiring emergency and hospital admissions for COPD. The effect of small airway dysfunction on the disease severity and control degree, disease phenotypes and quality of life, and the effect on the risk of exacerbation will be analyzed.

Interventions

DIAGNOSTIC_TESTImpulse oscillometry

Impulse oscillometry is a pulmonary function test. During the test, the participant is told to breathe normally.

In the spirometric pulmonary function test, the participant is asked to perform respiratory maneuvers such as breathing deeply.

In the FENO test, the participant is asked to perform respiratory maneuvers such as breathing deeply.

Computed tomography is a radiological examination.

DIAGNOSTIC_TESTChest X Ray

Chest X ray is a radiological examination.

DIAGNOSTIC_TESTBlood eosinophil level

A tube of blood will be drawn from the participant.

OTHERCAT

It consists of 8 questions.

OTHERmMRC

It is the scale used to measure the severity of shortness of breath.

Sponsors

Mersin University
CollaboratorOTHER
Sibel Naycı
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

COPD group * Participants who applied to the chest diseases clinic of Mersin University Hospital, between October 1, 2019 and April 1, 2020 * Participants who were diagnosed COPD with spirometry test * Reading and signing Informed Consent Form * Participants must be older than 18 years Healthy control group with a history of smoking * To apply to the chest diseases clinic of Mersin University Hospital between October 1, 2019 and April 1, 2020 * Reading and signing informed consent form * Participants must be older than 18 years * Must have no lung disease * Must have 10 packs / year or more than 10 packs / year smoking history Healthy control group without smoking history * To apply to the chest diseases clinic of Mersin University Hospital between October 1, 2019 and April 1, 2020 * Reading and signing informed consent form * Participants must be older than 18 years * Must have no lung disease * Must have no smoking history

Exclusion criteria

* Participants who do not sign the Informed Consent Form * Under the age of 18 years * Pregnant women * Participants who with a history of cancer in the past 5 years * Participants who previously had lung surgery * Participants who with Interstitial Lung Disease * Participants who with respiratory muscle disease * Participants who with active pulmonary tuberculosis * Participants who can not perform respiratory function tests

Design outcomes

Primary

MeasureTime frameDescription
Forced expiratory volume in 1 second (fev1) change will be evaluated by spirometric pulmonary function test.through study completion, an average of 1 yearForced expiratory volume in 1 second (fev1) change over one year period will be evaluated with spirometric pulmonary function test during recruitment and 1st year of follow-up.
Small airway dysfunction will be evaluated by body plethysmography test.through study completion, an average of 1 yearResidual volume (RV) and total lung capacity (TLC) will be measured by body plethysmography test to determine small airway dysfunction.
Symptoms will be evaluated by Modified Medical Research Council Dyspnea Scale (mMRC).through study completion, an average of 1 yearThe mMRC (Modified Medical Research Council) scale is a self-rating tool to measure the degree of disability that breathlessness poses on day-to-day activities on a scale from 0 to 4: 0, no breathlessness except on strenuous exercise; 1, shortness of breath when hurrying on the level or walking up a slight hill; 2, walks slower than people of same age on the level because of breathlessness or has to stop to catch breath when walking at their own pace on the level; 3, stops for breath after walking ∼100 m or after few minutes on the level; and 4, too breathless to leave the house, or breathless when dressing or undressing.
The number of moderate and severe exacerbations over a 1 year period will be recorded.through study completion, an average of 1 yearIn the COPD group, each participant will be followed for 1 year in terms of recording exacerbations.
Small airway dysfunction will be evaluated by performing impulse oscillometry test.through study completion, an average of 1 yearRespiratory resistance at 5 and 20 Hz (R5 and R20, respectively) will be used for the analyses. R5 and R20 are regarded as reflecting total and proximal airway resistance, respectively, and the fall in resistance from R5 to R20 (R5-R20) will used as a surrogate for the resistance of small airways.
Small airway dysfunction will be evaluated by thorax computed tomography.through study completion, an average of 1 yearIndirect changes caused by the small airways on the lung parenchyma will be detected by computed tomography (CT).

Secondary

MeasureTime frameDescription
Complete blood count ( CBC) test will be used as an indicator of inflammation.through study completion, an average of 1 yearBlood eosinophil levels will be recorded.
Quality of life will be evaluated by COPD Assessment Test (CAT).through study completion, an average of 1 yearCOPD Assessment Test (CAT) contains 8 questions. In each question, the minimum value is zero and the maximum value is five points. Higher score means worse outcome.
Fractional Exhaled Nitric Oxide (FENO) test will be used as an indicator of inflammation.through study completion, an average of 1 yearFENO test is indirect measurements of inflammation, as used in clinical practice.

Countries

Turkey (Türkiye)

Outcome results

None listed

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