Skip to main content
OpenTrials
Completed

NCT Number: NCT03372473

Montelukast and Loratadine in Children With Asthma

Randomized controlled trial in 80 children with mild to persistent moderate asthma, who were randomized to receive montelukast 5mg + loratadine 5mg vs. montelukast 5mg + placebo for loratadine to evaluate the efficacy in terms of improvement of symptoms. Secondary outcome was the days off without the use of rescue medication; reduction of levels of cysteinyl leukotrienes (Cys-LTS), nitric oxide (FeNO), intracellular adhesion molecule type 1 (ICAM-1) and interleukin 8 (IL-8) in condensed exhaled air; the improvement of day and night symptoms; the reduction in the frequency of night awakenings; the improvement in the quality of life; the percentage of related adverse events; the need to use systemic steroids; the number of visits to the emergency department secondary to the presence of an asthma attack; the number of hospitalizations secondary to asthma attacks; and the improvement in the percentage of FEV1 in relation to the predicted.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

6 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

About this study

Asthma is a disease with increasing prevalence worldwide that produces significant deterioration of the quality of life in children and development of important complications and economic, social impact. Considering the concept of a common airway (coexistence of asthma and rhinitis), joint management initiatives with anti-asthmatics and anti-histamines have been published. The primary objective of this clinical trial is to evaluate the efficacy and safety of the use of montelukast + loratadine in children with asthma on the improvement of symptoms and secondarily to evaluate the impact on a) the days off without the use of rescue medication; b) reduction of levels of cysteinyl leukotrienes (Cys-LTS), nitric oxide (FeNO), intracellular adhesion molecule type 1 (ICAM-1) and interleukin 8 (IL-8) in condensed exhaled air; c) the improvement of day and night symptoms; d) the reduction in the frequency of night awakenings; e) the improvement in the quality of life; f) the percentage of related adverse events; g) the need to use systemic steroids; h) the number of visits to the emergency department secondary to the presence of an asthma attack; i) the number of hospitalizations secondary to asthma attacks; and j) the improvement in the percentage of FEV1 in relation to the predicted. We included 80 children from 6 to 12 years old, any sex, with mild to moderate persistent asthma, after signing an informed consent letter by parents or guardians or signing the child's consent (> 8 years). Children with chronic diseases associated with the disease of interest were excluded (heart disease, nephropathy, liver disease of any kind); with any other lung disease other than asthma; with a history of hypersensitivity to montelukast or loratadine or with a history of concomitant use of medications that interact significantly with montelukast or loratadine

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age from 6 to 12 years old
  • Any sex
  • Persistent mild to moderate asthma
  • Signature of informed consent letter by parents or guardians
  • Letter of assent of the minor for children over 9 years of age

Exclusion criteria

  • Chronic pathologies associated with the disease of interest (heart disease, nephropathy, liver disease of any kind)
  • Any other lung disease other than asthma
  • History of hypersensitivity to montelukast or loratadine
  • Concomitant use of medications that interact significantly with montelukast or loratadine

Treatment and study plan

Montelukast mixed with Loratadine

Drug

Montelukast 5mg mixed with Loratadine 5mg, one dose per day

Montelukast

Drug

Montelukast 5mg

Primary outcomes

  1. Free of symptoms

    Time frame: 10 weeks

    Number of days free of symptoms associated to asthma episodes

Secondary outcomes

  1. Free of rescue medication

    Time frame: 10 weeks

    Number of days free for use of rescue medications

  2. Reduction of airway inflammatory profile

    Time frame: 10 weeks

    Measurement of inflamatory biomarkers in exhaled respiratory air

  3. Reduction of awakenings

    Time frame: 10 weeks

    Frequency of nocturn awakenings

  4. Quality of Life

    Time frame: 10 weeks

    Changes in PedsQL during the treatment

  5. Emergency visits

    Time frame: 10 weeks

    Number of emergency visits secondary to asthma crisis

  6. Adverse Events

    Time frame: 10 weeks

    Frequency of reported adverse events

Sponsors and collaborators

Lead sponsor

Innovacion y Desarrollo de Estrategias en Salud

Other

Collaborators

  • Laboratorios Senosiain, S.A. de C.V.
  • National Institute of Pediatrics, Mexico

Registry information

Official study title

Safety and Efficacy of Montelukast + Loratadine vs. Montelukast for the Control of Mild to Moderate Persistent Asthma in Children: Randomized Controlled Clinical Trial

Important dates

Study start
2016
Primary completion
2016
Study completion
2017
First posted
Dec 13, 2017
Registry last updated
Dec 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.