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

11 augusti 2020 uppdaterad av: Henryk Mazurek, National Institute for Tuberculosis and Lung Diseases, Poland

Adjustment of Asthma Treatment in Children Based on an Indirect Hyperresponsiveness Test - a Randomized Trial

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.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Faktisk)

108

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Lesko, Polen, 38-600
        • The Regional Public Hospital in Lesko, Poland

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

7 år till 15 år (Barn)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Grundläggande vetenskap
  • Tilldelning: Randomiserad
  • Interventionsmodell: Faktoriell uppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Inget ingripande: symptoms group
The asthma treatment adjustments guided by GINA guidelines
Experimentell: BHR group
The asthma treatment adjustments additionally taking account to the results of the bronchial hyperresponsiveness test
Modification of inhaled corticosteroid dose based on the symptoms and the result of bronchial provocation (BHR group)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
asthma exacerbations
Tidsram: 12 months
number of asthma exacerbations
12 months

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
the percentage of participants with asthma exacerbations
Tidsram: 12 months
the number of patients with at least 1 exacerbation divided by the number of patients in each group
12 months
time to the first asthma exacerbation
Tidsram: 12 months
the median time to the first asthma exacerbation in each group
12 months
ICS dose
Tidsram: 12 months
the final dose of ICS
12 months
days with symptoms
Tidsram: 12 months
total number of days with asthma symptoms
12 months
days with asthma medication
Tidsram: 12 months
total number of days with bronchodilator use
12 months
blood eosinophilia
Tidsram: 12 months
number of blood eosinophils
12 months
exhaled nitric oxide
Tidsram: 12 months
orally exhaled nitric oxide concentration
12 months
spirometry
Tidsram: 12 months
FEV1, forced vital capacity (FVC) and FEF (MMEF) values
12 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Allmänna publikationer

Användbara länkar

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

2 juli 2018

Primärt slutförande (Faktisk)

30 augusti 2019

Avslutad studie (Faktisk)

30 augusti 2019

Studieregistreringsdatum

Först inskickad

7 augusti 2020

Först inskickad som uppfyllde QC-kriterierna

11 augusti 2020

Första postat (Faktisk)

12 augusti 2020

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

12 augusti 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

11 augusti 2020

Senast verifierad

1 augusti 2020

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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