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Adjustment of Asthma Treatment in Children Based on an Indirect Hyperresponsiveness Test

Not Applicable
Completed
Conditions
Asthma in Children
Interventions
Other: asthma treatment adjustment taking account on degree of bronchial hyperresponsiveness
Registration Number
NCT04509921
Lead Sponsor
National Institute for Tuberculosis and Lung Diseases, Poland
Brief Summary

The aim of the study is to assess the usefulness of the indirect bronchial hyperresponsiveness test (with hypertonic NaCl) in determining the optimal dose of inhaled steroids to maintain asthma control.

The study was designed as a prospective, real-life, randomized, interventional study. This single-site study is performed at the Allergology Clinic in Lesko.

The study included participants aged 7-15 years who met the eligibility criteria. Eligible participants were selected from a pool of 231 patients with mild asthma, under the care of the Allergology Clinic of the Regional Public Hospital in Lesko (Poland). All participants were diagnosed with chronic mild asthma for at least two years.

Subjects initially enrolled in the study had good asthma control maintained for at least 3 months on low / medium-dose ICS monotherapy, with no exacerbations requiring systemic corticosteroids in the previous 3 months, no respiratory tract infection in last month, and an FEV1 above 80% expected.

Finally, 108 children were enrolled in the study. They were aged 7-15 years, with active mild asthma, confirmed by the presence of bronchial hyperreactivity and symptoms of asthma, emerging after discontinuation of anti-inflammatory treatment.

Participation in the study lasted one year.

The study includes:

4-week run-in period (withdrawal phase) after discontinuation of anti-inflammatory treatment (ICS) with clinical symptoms and medication use recording, completed by the patient and parents.

At the end of this period, spirometry was performed, bronchial hyperreactivity was assessed with the hyperosmolar salt provocation, and the parameters of inflammation were measured: orally exhaled nitric oxide concentration (NO) and peripheral blood eosinophilia. The anti-inflammatory treatment was then resumed (with ICS in the previous doses).

Only patients with active asthma and increased bronchial responsiveness (DRS\>0.55) were qualified for the main study. Stratified randomization was performed for age, clinical symptoms, and the degree of bronchial hyperresponsiveness. On this basis, the division into 2 research groups was made:

* a symptom-only monitored treatment group

* a group in which therapy changes were based on the symptoms and degree of bronchial hyperresponsiveness (BHR group).

Patients/parents were provided by an established algorithm for managing asthma symptoms/exacerbations. In the case of loss of asthma control, a beta-agonist was administered (temporarily) and the dose of ICS quadrupled. Patients had the possibility of additional visits - if necessary. Especially, severe exacerbations were verified by the attending physician, and on this basis, oral steroids would be considered.

Throughout the study, the participants kept daily observation charts (clinical symptoms and drug use) and peak expiratory flow rate (PEFR) measurements.

The telephone report was made monthly with the number of days with asthma symptoms and medications used, and this was recorded in the documentation of the study.

The clinical evaluation was performed every 3 months with symptom evaluation, spirometry, exhaled NO, peripheral blood eosinophilia, and BHR measurements (half of the patients).

The treatment adjustments were guided by the patient's and parent's reporting of symptoms, and additionally by the results of periodic clinical assessment (including the assessment of bronchial hyperresponsiveness in the BHR group). This means that the level of treatment intensity (ICS dose) was based on symptom monitoring only in the observation group, and additionally took into account the level of bronchial responsiveness in the BHR monitoring group.

The study was completed after one year of follow-up (4 visits every 3 months). The primary endpoint of the study: the number of asthma exacerbations in both study arms.

Secondary endpoints:

* days with symptoms

* asthma medication days

* final dose of ICS

* spirometry (FEV1, MMEF)

* bronchial hyperreactivity (BHR group only)

* nitric oxide in the exhaled air

* peripheral blood eosinophilia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
108
Inclusion Criteria
  • mild asthma with a stable course of at least 3 months
  • good adherence to treatment with low dose ICS
Exclusion Criteria
  • infection or exacerbation of asthma requiring the use of systemic steroids (or changes in the dose of inhaled steroids) in the last 3 months before the study
  • other chronic lung diseases or general diseases affecting the respiratory system
  • tobacco smoking
  • FEV1 below 80% of the predicted value

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
BHR groupasthma treatment adjustment taking account on degree of bronchial hyperresponsivenessThe asthma treatment adjustments additionally taking account to the results of the bronchial hyperresponsiveness test
Primary Outcome Measures
NameTimeMethod
asthma exacerbations12 months

number of asthma exacerbations

Secondary Outcome Measures
NameTimeMethod
the percentage of participants with asthma exacerbations12 months

the number of patients with at least 1 exacerbation divided by the number of patients in each group

time to the first asthma exacerbation12 months

the median time to the first asthma exacerbation in each group

ICS dose12 months

the final dose of ICS

days with symptoms12 months

total number of days with asthma symptoms

days with asthma medication12 months

total number of days with bronchodilator use

blood eosinophilia12 months

number of blood eosinophils

exhaled nitric oxide12 months

orally exhaled nitric oxide concentration

spirometry12 months

FEV1, forced vital capacity (FVC) and FEF (MMEF) values

Trial Locations

Locations (1)

The Regional Public Hospital in Lesko, Poland

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Lesko, Poland

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