Asthma Clinical Trial
Official title:
The Prevalence Of Small Airways Dysfunction In Asthma Patients And The Impact On The Asthma Control
Verified date | May 2020 |
Source | Mersin University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Asthma, which are one of the most important causes of morbidity and mortality both in the world and in our country, constitute a very serious social and economic burden. An estimated 300 million people suffer from asthma worldwide, which is a major public health problem. Asthma is complex and heterogeneous chronic airway diseases that require a multifaceted approach. In asthma, small airways represent key regions of airflow obstruction. Although small airway dysfunction 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. Thus, there is an unmet need to assess its role in the control of the disease. Therefore, our primary aim in the study is to determine the frequency of small airway dysfunction measured by impulse oscillometry in Asthma patients. 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 Asthma.
Status | Active, not recruiting |
Enrollment | 108 |
Est. completion date | April 1, 2021 |
Est. primary completion date | September 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Asthma 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 asthma with spirometry test - Reading and signing Informed Consent Form - Participants must be older than 18 years Healthy control group - 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 |
Country | Name | City | State |
---|---|---|---|
Turkey | Mersin University Faculty of Medicine, Department of Respiratory Diseases | Mersin | Yenisehir |
Lead Sponsor | Collaborator |
---|---|
Sibel Nayci | Mersin University |
Turkey,
Postma DS, Brightling C, Baldi S, Van den Berge M, Fabbri LM, Gagnatelli A, Papi A, Van der Molen T, Rabe KF, Siddiqui S, Singh D, Nicolini G, Kraft M; ATLANTIS study group. Exploring the relevance and extent of small airways dysfunction in asthma (ATLANTIS): baseline data from a prospective cohort study. Lancet Respir Med. 2019 May;7(5):402-416. doi: 10.1016/S2213-2600(19)30049-9. Epub 2019 Mar 12. Erratum in: Lancet Respir Med. 2019 Sep;7(9):e28. — View Citation
Usmani OS, Singh D, Spinola M, Bizzi A, Barnes PJ. The prevalence of small airways disease in adult asthma: A systematic literature review. Respir Med. 2016 Jul;116:19-27. doi: 10.1016/j.rmed.2016.05.006. Epub 2016 May 7. Review. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Small airway dysfunction will be evaluated by performing impulse oscillometry test. | We will used respiratory resistance at 5 and 20 Hz (R5 and R20, respectively) 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. | through study completion, an average of 1 year | |
Primary | Small airway dysfunction will be evaluated by thorax computed tomography. | Indirect changes caused by the small airways on the lung parenchyma will be detected by computed tomography (CT). | through study completion, an average of 1 year | |
Primary | Small airway dysfunction will be evaluated by body plethysmography test. | Residual volume (RV) and total lung capacity (TLC) will be measured by body plethysmography test to determine small airway dysfunction. | through study completion, an average of 1 year | |
Primary | Symptom control will be evaluated by asthma control test. | The asthma control test consists of 5 questions. | through study completion, an average of 1 year | |
Primary | The number of moderate and severe exacerbations over a 1 year period will be recorded. | In the asthma group, each participant will be followed for 1 year in terms of recording exacerbations. | through study completion, an average of 1 year | |
Primary | Forced expiratory volume in 1 second (fev1) change will be evaluated by spirometric pulmonary function test. | Forced 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. | through study completion, an average of 1 year | |
Secondary | Quality of life will be evaluated by Asthma Quality of Life Questionnaire (AQLQ). | Asthma Quality of Life Questionnaire (AQLQ) contains 32 questions. | through study completion, an average of 1 year | |
Secondary | Fractional Exhaled Nitric Oxide (FENO) test will be used as an indicator of inflammation in determining the relationship between airway inflammation and small airway dysfunction. | FENO test is indirect measurements of inflammation, as used in clinical practice. | through study completion, an average of 1 year | |
Secondary | The relationship between blood inflammation cells and small airway dysfunction will be evaluated by complete blood count ( CBC). | Blood eosinophil and neutrophil levels will be recorded. | through study completion, an average of 1 year |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04624425 -
Additional Effects of Segmental Breathing In Asthma
|
N/A | |
Terminated |
NCT04410523 -
Study of Efficacy and Safety of CSJ117 in Patients With Severe Uncontrolled Asthma
|
Phase 2 | |
Active, not recruiting |
NCT03927820 -
A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)
|
N/A | |
Completed |
NCT04617015 -
Defining and Treating Depression-related Asthma
|
Early Phase 1 | |
Recruiting |
NCT03694158 -
Investigating Dupilumab's Effect in Asthma by Genotype
|
Phase 4 | |
Terminated |
NCT04946318 -
Study of Safety of CSJ117 in Participants With Moderate to Severe Uncontrolled Asthma
|
Phase 2 | |
Completed |
NCT04450108 -
Vivatmo Pro™ for Fractional Exhaled Nitric Oxide (FeNO) Monitoring in U.S. Asthmatic Patients
|
N/A | |
Completed |
NCT03086460 -
A Dose Ranging Study With CHF 1531 in Subjects With Asthma (FLASH)
|
Phase 2 | |
Completed |
NCT01160224 -
Oral GW766944 (Oral CCR3 Antagonist)
|
Phase 2 | |
Completed |
NCT03186209 -
Efficacy and Safety Study of Benralizumab in Patients With Uncontrolled Asthma on Medium to High Dose Inhaled Corticosteroid Plus LABA (MIRACLE)
|
Phase 3 | |
Completed |
NCT02502734 -
Effect of Inhaled Fluticasone Furoate on Short-term Growth in Paediatric Subjects With Asthma
|
Phase 3 | |
Completed |
NCT01715844 -
L-Citrulline Supplementation Pilot Study for Overweight Late Onset Asthmatics
|
Phase 1 | |
Terminated |
NCT04993443 -
First-In-Human Study to Evaluate the Safety, Tolerability, Immunogenicity, and Pharmacokinetics of LQ036
|
Phase 1 | |
Completed |
NCT02787863 -
Clinical and Immunological Efficiency of Bacterial Vaccines at Adult Patients With Bronchopulmonary Pathology
|
Phase 4 | |
Recruiting |
NCT06033833 -
Long-term Safety and Efficacy Evaluation of Subcutaneous Amlitelimab in Adult Participants With Moderate-to-severe Asthma Who Completed Treatment Period of Previous Amlitelimab Asthma Clinical Study
|
Phase 2 | |
Completed |
NCT03257995 -
Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of Two Orally Inhaled Indacaterol Salts in Adult Subjects With Asthma.
|
Phase 2 | |
Completed |
NCT02212483 -
Clinical Effectiveness and Economical Impact of Medical Indoor Environment Counselors Visiting Homes of Asthma Patients
|
N/A | |
Recruiting |
NCT04872309 -
MUlti-nuclear MR Imaging Investigation of Respiratory Disease-associated CHanges in Lung Physiology
|
||
Withdrawn |
NCT01468805 -
Childhood Asthma Reduction Study
|
N/A | |
Recruiting |
NCT05145894 -
Differentiation of Asthma/COPD Exacerbation and Stable State Using Automated Lung Sound Analysis With LungPass Device
|