A Phase 4 interventional study of Montelukast and Placebo in Asthma, sponsored by PharmEvo Pvt Ltd. Completed at 1 site in Pakistan. Open to participants aged 15 Years and older. Per ClinicalTrials.gov, last updated 2018-07-09.
Sponsored by PharmEvo Pvt Ltd · Phase 4, Interventional, and Treatment
1.1 Background
Asthma is characterized by airway and lung tissue inflammation and airway hyperresponsiveness (AHR) that leads to recurrent symptoms of wheezing, breathlessness, chest tightness, and coughing. AHR indicates an exaggerated response of the airway to nonspecific stimuli, which results in a temporary airflow limitation, leading to airway obstruction. It remains unknown which factors within the airway of an individual trigger reversible airway obstruction and airway narrowing. The airway epithelium is composed of many interacting structural components and inflammatory cells. The number, activation, and secretory component of inflammatory cells in the airway are altered in the disease. In asthma, the number of eosinophils and T lymphocytes is increased in the subepithelial layer.
The impact of asthma has traditionally been measured in terms of the prevalence of the disease, mortality rates, and levels of healthcare utilisation, particularly hospital admissions. However, the impact of asthma extends beyond these outcomes to include effects on lifestyle, wellbeing, and perceived health status. Adults of working age with asthma have poorer health status and quality of life outcomes than those with no asthma. This effect is independent of confounding by sociodemographic and life style factors and is evident across a range of dimensions of quality of life. In comparison with two other chronic health conditions, asthma has a larger adverse impact on health status and quality of life than diabetes.
1.2. Investigational Agent
Montelukast reversibly inhibits cysteinyl leukotrienes (CysLTs), specifically leukotrienes D4 (LTD4 [3]. LTD4 is the most potent bronchoconstricting agent on a molar basis, but Cys-LTs also have chemoattractive properties for many inflammatory cells (mainly eosinophils), effects on vascular permeability, mucous secretions and sensory nerve activation, and are responsible for part of the pathophysiology of asthma.
1.3. Dose Rational/Risk \& Benefit
Montelukast is a potent and selective blocker of the CysLT1 receptor. For treatment of chronic asthma, montelukast is administered once daily to adults as a 10-mg film-coated tablet, to children aged 6-14 years as a 5-mg chewable tablet, and to children aged 2-5 years as a 4-mg chewable tablet form. Given their efficacy, antiinflammatory activity, oral administration, and safety, leukotriene modifiers will play an important role in the treatment of asthmatic patient. Side effects most commonly reported above placebo included headache, otitis media, upper respiratory infection, and pharyngitis.
3,921 studies on the registry are indexed under Asthma; 506 are open to participants now.
This study's enrollment of 180 is above the median of 83 across 2,751 interventional studies indexed under Asthma.
Browse Asthma studies →PharmEvo Pvt Ltd is the lead sponsor of 8 studies on the registry; none are open to participants now.
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Exclusion Criteria:
Aireez contains Montelukast which is a potent and selective blocker of the CysLT1 receptor. For treatment of chronic asthma, montelukast is administered once daily to adults as a 10-mg film-coated tablet, to children aged 6-14 years as a 5-mg chewable tablet, and to children aged 2-5 years as a 4-mg chewable tablet form.
Drug: Montelukast
Patients in placebo group will receive identical looking drug (placebo) produced by same manufactured.
Drug: Placebo
Montelukast sodium is a selective blocker of the CysLT1 receptor. For treatment of chronic asthma, montelukast is administered once daily to adults as a 10-mg film-coated tablet, to children aged 6-14 years as a 5-mg chewable tablet, and to children aged 2-5 years as a 4-mg chewable tablet form.
Also known as: TEAM
Patients in placebo group will receive identical looking drug (placebo) produced by same manufactured
Also known as: TEAM
To assess the change in quality of Life using AQLQ (s) questionnaire after 4 weeks of Montelukast.
\[Designated as safety issue: No\]
Time frame: 0 days to 4 weeks
To assess the change in Control of Asthma using AQLQ (s) questionnaire after 4 weeks of Montelukast.
\[Designated as safety issue: No\]
Time frame: 0 days to 4 weeks
Proportion of participants experiencing an adverse event (AE)
\[Designated as safety issue: Yes\]
Time frame: 0 days to 4 weeks
Plan to share: No
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This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.
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