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

11 de agosto de 2020 actualizado por: 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.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

108

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

7 años a 15 años (Niño)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Ciencia básica
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación factorial
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Sin intervención: symptoms group
The asthma treatment adjustments guided by GINA guidelines
Experimental: 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)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
asthma exacerbations
Periodo de tiempo: 12 months
number of asthma exacerbations
12 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
the percentage of participants with asthma exacerbations
Periodo de tiempo: 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
Periodo de tiempo: 12 months
the median time to the first asthma exacerbation in each group
12 months
ICS dose
Periodo de tiempo: 12 months
the final dose of ICS
12 months
days with symptoms
Periodo de tiempo: 12 months
total number of days with asthma symptoms
12 months
days with asthma medication
Periodo de tiempo: 12 months
total number of days with bronchodilator use
12 months
blood eosinophilia
Periodo de tiempo: 12 months
number of blood eosinophils
12 months
exhaled nitric oxide
Periodo de tiempo: 12 months
orally exhaled nitric oxide concentration
12 months
spirometry
Periodo de tiempo: 12 months
FEV1, forced vital capacity (FVC) and FEF (MMEF) values
12 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

2 de julio de 2018

Finalización primaria (Actual)

30 de agosto de 2019

Finalización del estudio (Actual)

30 de agosto de 2019

Fechas de registro del estudio

Enviado por primera vez

7 de agosto de 2020

Primero enviado que cumplió con los criterios de control de calidad

11 de agosto de 2020

Publicado por primera vez (Actual)

12 de agosto de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de agosto de 2020

Última actualización enviada que cumplió con los criterios de control de calidad

11 de agosto de 2020

Última verificación

1 de agosto de 2020

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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