Effect of Montelukast in Asthma in Children
Primary Purpose
Bronchial Asthma
Status
Unknown status
Phase
Phase 3
Locations
Poland
Study Type
Interventional
Intervention
Montelukast sodium.
Placebo tablet and budesonide
Sponsored by

About this trial
This is an interventional treatment trial for Bronchial Asthma focused on measuring asthma; children; montelukast; treatment; exacerbation
Eligibility Criteria
Inclusion Criteria:
- Children with bronchial asthma
Exclusion Criteria:
- All other serious diseases
Sites / Locations
- Department of Pediatrics and Allergy, Medical University of Lodz, N. Copernicus HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
montelukast group
Placebo group
Arm Description
Children with asthma treated with montelukast and budesonide.
Children with asthma treated with placebo tablet and budesonide.
Outcomes
Primary Outcome Measures
Steroid dose,medium steroid dose/day,number of asthma exacerbations,maximum fall of FEV1 in exercise, asthma symptoms, lung function, number of patients with positive airway hyperresponsiveness
steroid doses sufficient to control asthma symptoms
medium steroid dose/day times 6 month
number of asthma exacerbations in 9 month period
maximum fall of FEV1 in exercise induced bronchoconstriction test
asthma symptoms scale and lung function
number of patients with positive airway hyperresponsiveness test
Secondary Outcome Measures
Full Information
NCT ID
NCT01266772
First Posted
December 23, 2010
Last Updated
February 6, 2013
Sponsor
Medical University of Lodz
1. Study Identification
Unique Protocol Identification Number
NCT01266772
Brief Title
Effect of Montelukast in Asthma in Children
Official Title
The Effect of Montelukast on Anti-inflammatory Treatment and Asthma Exacerbation Prevention in Children Sensitive to Dust Mites.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
January 2011 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Lodz
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This is 9 month, placebo-controlled, double blind, randomised trial using the oral leucotrienes receptor antagonist montelukast (5 mg) in 160 children with mild and moderate asthma age 6-14 year old, sensitive to house dust mite. There are two study groups: montelukast group 80 patients and placebo group 80 patients. All patients will receive budesonide in dose sufficient to control asthma symptoms and short-acting beta agonist as needed. Medication used in the study: montelukast 5mg, budesonide. There are 7 doctor's visits - one initial visit (June) and 6 follow-up visits. First visit is on the first day of asthma symptom and each follow-up visit is every 6 weeks. Children with full asthma control (as measured by exhaled NO) had administered 100 mcg lower dose of budesonide and children with not fully control asthma had administered 100 mcg higher dose of budesonide.
Detailed Description
The most potent anti-inflammatory drugs in asthma are glucocorticosteroids. Corticosteroids, however have side effects and do not fully suppress the production or release of all inflammatory mediators. Amongst those less affected are cysteinyl leucotrienes, which are known to play a key role in asthma. Antileucotrienes have a bronchodilator and bronchoprotective potential and have thus became part of current treatment recommendations in asthma.
Owing to the beneficial effects of antileucotrienes and the efforts to keep steroid doses low, our study address the extent to which inhaled corticosteroids might be substituted or supplemented by these drugs. We used symptoms, frequency of exacerbation, exercise induced bronchoconstriction test, and exhaled NO during a stepwise reduction of steroid doses to assess the association between these variables and their relation to the patients' clinical benefit; we used airway hyperresponsiveness to assess inflammatory process in airways.
This is 9 month, placebo-controlled, double blind, randomised trial using the oral leucotrienes receptor antagonist montelukast (5 mg) in 160 children with mild and moderate asthma age 6-14 year old, sensitive to house dust mite. There are two study groups: montelukast group 80 patients and placebo group 80 patients. All patients will receive budesonide in dose sufficient to control asthma symptoms and short-acting beta agonist as needed. Medication used in the study: montelukast 5mg, budesonide. There are 7 doctor's visits - one initial visit (June) and 6 follow-up visits. First visit is on the first day of asthma symptom and each follow-up visit is every 6 weeks. Children with full asthma control (as measured by exhaled NO) had administered 100 mcg lower dose of budesonide and children with not fully control asthma had administered 100 mcg higher dose of budesonide.
Methods used in the study:
doctor's exam
asthma symptoms questionaire
exhaled NO
spirometry
exercise induced bronchoconstriction test
airway hyperresponsiveness test
End points:
steroid doses sufficient to control asthma symptoms
medium steroid dose/day times 6 month
number of asthma exacerbations in 9 month period
maximum fall of FEV1 in exercise induced bronchoconstriction test
asthma symptoms scale and lung function
number of patients with positive airway hyperresponsiveness test
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchial Asthma
Keywords
asthma; children; montelukast; treatment; exacerbation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
montelukast group
Arm Type
Active Comparator
Arm Description
Children with asthma treated with montelukast and budesonide.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Children with asthma treated with placebo tablet and budesonide.
Intervention Type
Drug
Intervention Name(s)
Montelukast sodium.
Other Intervention Name(s)
Montelukast and Budesonide
Intervention Description
Children with asthma treated with montelukast and budesonide.
Intervention Type
Drug
Intervention Name(s)
Placebo tablet and budesonide
Other Intervention Name(s)
Placebo tablet and Budesonide.
Intervention Description
Children with asthma treated with placebo tablet and budesonide.
Primary Outcome Measure Information:
Title
Steroid dose,medium steroid dose/day,number of asthma exacerbations,maximum fall of FEV1 in exercise, asthma symptoms, lung function, number of patients with positive airway hyperresponsiveness
Description
steroid doses sufficient to control asthma symptoms
medium steroid dose/day times 6 month
number of asthma exacerbations in 9 month period
maximum fall of FEV1 in exercise induced bronchoconstriction test
asthma symptoms scale and lung function
number of patients with positive airway hyperresponsiveness test
Time Frame
9 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children with bronchial asthma
Exclusion Criteria:
All other serious diseases
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Agata Ożarek-Hanc, MD
Phone
0048426895972
Email
alergol@kopernik.lodz.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agata Ożarek-Hanc, MD
Organizational Affiliation
Department of Pediatrics and Allergy, Medical University of Lodz, N. Copernicus Hospital, Lodz, Poland.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Iwona Stelmach, Prof.
Organizational Affiliation
Department of Pediatrics and Allergy, Medical University of Lodz, N. Copernicus Hospital, Lodz, Poland
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Pediatrics and Allergy, Medical University of Lodz, N. Copernicus Hospital
City
Lodz
ZIP/Postal Code
93-513
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Iwona Stelmach, Prof.
Email
alergol@kopernik.lodz.pl
First Name & Middle Initial & Last Name & Degree
Agata Ożarek-Hanc, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
25640020
Citation
Stelmach I, Ozarek-Hanc A, Zaczeniuk M, Stelmach W, Smejda K, Majak P, Jerzynska J, Anna J. Do children with stable asthma benefit from addition of montelukast to inhaled corticosteroids: randomized, placebo controlled trial. Pulm Pharmacol Ther. 2015 Apr;31:42-8. doi: 10.1016/j.pupt.2015.01.004. Epub 2015 Jan 30.
Results Reference
derived
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Effect of Montelukast in Asthma in Children
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