Effect of Montelukast on Remodelling Markers in Asthmatic Children (MORACH)
Primary Purpose
Asthma
Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Montelukast
placebo
Sponsored by

About this trial
This is an interventional basic science trial for Asthma focused on measuring Asthma, Children, Remodelling, Metalloproteinases, Montelukast
Eligibility Criteria
Inclusion Criteria:
- Diagnostic criteria: the classification of asthma will be based on clinical history and examination and pulmonary function parameters, according to international guidelines.
- Stage and/or severity of condition: atopic children with mild intermittent asthma will be enrolled. Atopy will be evaluated by skin-prick test to common allergens in the area.
- Confirmatory physical and laboratory findings:
- Age: ranging in age 6 to 14 years.
- Evidence of susceptibility to the disease under study
- Patients have not used ICS during 3-month period prior to study entry
Exclusion Criteria:
- Patients will be excluded if they had used oral steroids in the last month.
- Patients will be excluded if they had acute or chronic lung diseases other than asthma, upper or lower airway infection in the previous 3 weeks or during the trial, acute asthma exacerbation, or had used oral steroids in the last month.
- Patients will be excluded if they had acute or chronic lung diseases other than asthma, upper or lower airway infections in the previous 3 weeks or during the trial, acute asthma exacerbation, or had used oral steroids in the last month.
Sites / Locations
- Pediatric Department, University of Verona
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Montelukast
placebo
Arm Description
Montelukast chewing tablets once daily per os, plus inhaled short acting beta2 agonist as needed
placebo chewing tablets per os once daily, plus inhaled short acting beta 2 agonist as needed
Outcomes
Primary Outcome Measures
FeNo, Lung Function, MMP-9, MMP-12, TIMP-1, PICP and TGFB determination
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00875082
Brief Title
Effect of Montelukast on Remodelling Markers in Asthmatic Children
Acronym
MORACH
Official Title
Effect of Montelukast on Metalloproteinase (MMP)-9, MMP-12, Tissue Inhibitor Metalloproteinase-1 (TIMP-1), Procollagen Type I C-terminal Peptide (PICP) and TGF-beta1 Levels in Sputum From Mild Intermittent Asthmatic Children: a Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universita di Verona
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Airway smooth muscle cell layer thickening and sub epithelial fibrosis, key allergen-induced airway remodelling features not modulated by corticosteroids, are reversible by CysLT1 receptor blockade therapy in animals. No data are available, at the present, about the potential effect of LTs receptor antagonists on airway remodelling in asthmatic children.
In the present study, the investigators aim to assess whether the addition of montelukast to ICS in mild asthmatic children to inhibit the release of MMP-9, TIMP-1, MMP-12, MMP-9/TIMP1 ratio, procollagen type I C-terminal peptide (PICP) and TGF-beta in the airway fluid collected by induced sputum in asthmatic children. 30-40 atopic children with mild persistent asthma.
Children with asthma will be recruited and evaluated with a real life open label trial: they will be randomised into two groups at first visit (T1): 1) group A: in these patients montelukast tablets 5 mg and as needed beta agonist will be administered; 2) group B: in these patients beta agonist therapy only.
All children will be evaluated after 8 weeks (T2). They will be tested for lung function, FeNO, metalloproteinase (MMP)-9, MMP-12, tissue inhibitor metalloproteinase-1 (TIMP-1), procollagen type I C-terminal peptide (PICP) and TGF-beta1 levels in sputum.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma, Children, Remodelling, Metalloproteinases, Montelukast
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Montelukast
Arm Type
Active Comparator
Arm Description
Montelukast chewing tablets once daily per os, plus inhaled short acting beta2 agonist as needed
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo chewing tablets per os once daily, plus inhaled short acting beta 2 agonist as needed
Intervention Type
Drug
Intervention Name(s)
Montelukast
Intervention Description
Montelukast, chewing tablets 5mg, once daily, 8 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo chewing tablets once daily, plus inhaled short acting beta2 agonist as needed, 8 weeks
Primary Outcome Measure Information:
Title
FeNo, Lung Function, MMP-9, MMP-12, TIMP-1, PICP and TGFB determination
Time Frame
8 weeks
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:
Diagnostic criteria: the classification of asthma will be based on clinical history and examination and pulmonary function parameters, according to international guidelines.
Stage and/or severity of condition: atopic children with mild intermittent asthma will be enrolled. Atopy will be evaluated by skin-prick test to common allergens in the area.
Confirmatory physical and laboratory findings:
Age: ranging in age 6 to 14 years.
Evidence of susceptibility to the disease under study
Patients have not used ICS during 3-month period prior to study entry
Exclusion Criteria:
Patients will be excluded if they had used oral steroids in the last month.
Patients will be excluded if they had acute or chronic lung diseases other than asthma, upper or lower airway infection in the previous 3 weeks or during the trial, acute asthma exacerbation, or had used oral steroids in the last month.
Patients will be excluded if they had acute or chronic lung diseases other than asthma, upper or lower airway infections in the previous 3 weeks or during the trial, acute asthma exacerbation, or had used oral steroids in the last month.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Attilio L Boner, MD
Organizational Affiliation
Pediatric Department, Università di Verona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Department, University of Verona
City
Verona
ZIP/Postal Code
I-37134
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
27657514
Citation
Tenero L, Piazza M, Sandri M, Azzali A, Chinellato I, Peroni D, Boner A, Piacentini G. Effect of montelukast on markers of airway remodeling in children with asthma. Allergy Asthma Proc. 2016 Sep;37(5):77-83. doi: 10.2500/aap.2016.37.3978.
Results Reference
derived
Learn more about this trial
Effect of Montelukast on Remodelling Markers in Asthmatic Children
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