Asthma Clinical Trial
Official title:
Concurrent Improvement of Exhaled Nitric Oxide and FEF25-75 After Treatment With Inhaled Corticosteroid in Children With Controlled Asthma
Abnormal lung function and high exhaled nitric oxide (FeNO) have been reported in asymptomatic patients with asthma. The investigators aimed to assess whether FeNO and FEF25-75 improve concurrently after treatment with inhaled corticosteroid (ICS) in patients with controlled asthma. Geometric mean (GM) FeNO and spirometric values in patients 8 to 16 years of age who maintained asthma control without controller medication were compared with healthy controls and patients with uncontrolled asthma who were also not receiving controller medications. Patients with controlled asthma and high FeNO (> 25 ppb) were randomized to ICS treatment or to remain untreated. Changes in spirometric values and GM FeNO from baseline were evaluated after 6 weeks.
Current guideline-defined asthma control cannot be applied to the level of airway
inflammation because neither symptoms nor the results of basic pulmonary function tests can
reflect ongoing airway inflammation.Consequently, asymptomatic or minimally symptomatic
patients are usually considered to have controlled asthma even if they have subclinical
airway inflammation. Measures of airway inflammation are thus required to identify patients
with silent airway inflammation which does not manifest itself as symptoms or impaired lung
function. In addition, measurement should be easy to perform, reproducible, and associated
with a high degree of acceptance by patients. In this regard, the advent of FeNO
measurements represents a significant advance in monitoring airway inflammation of asthmatic
patients. High FeNO values above certain cut-point may indicate active eosinophilic airway
inflammation and the likelihood of deterioration in asthma control. However, it is still
unclear that high FeNO in asymptomatic patients implies the need for the anti-inflammatory
treatment.
Current guidelines for asthma management recommended forced expiratory volume in the first
second (FEV1) as a principle spirometric parameter to assess airflow limitation. However,
asthmatic subjects have air trapping in the presence of normal FEV1. Air trapping in
asthmatic subjects has been demonstrated to be better correlated with forced expiratory flow
between 25% and 75% of vital capacity % predicted (FEF25-75 % predicted) than FEV1 %
predicted. In fact, impaired FEF25-75 is one of the most common abnormalities in pulmonary
function in cross-sectional studies in asymptomatic patients. In addition, high FeNO in
asymptomatic or minimally symptomatic patients may be accompanied by impairment of FEF25-75
because both parameters have been suggested to be measures of residual small airway disease.
Therefore, there is a possibility that the improvement of FEF25-75 happens concomitantly
with the decrease of FeNO during the anti-inflammatory treatment. In this study, we
recruited previously well-documented atopic asthmatic children who required no medication to
maintain asthma control for more than 3 months and had high FeNO levels (> 25 ppb). We aimed
to assess whether the decrease of FeNO occurs simultaneously with improvement of FEF25-75
after treatment with inhaled corticosteroid (ICS) in these patients.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT04410523 -
Study of Efficacy and Safety of CSJ117 in Patients With Severe Uncontrolled Asthma
|
Phase 2 | |
| Completed |
NCT04624425 -
Additional Effects of Segmental Breathing In Asthma
|
N/A | |
| 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
|