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CompletedNCT03096327TEAMUpdated Jul 9, 2018

TEAM (Trial on Efficacy and Quality of Life Among Asthmatic Patient With Montelukast)

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

Phase
Phase 4
Study type
Interventional
Enrollment
180
Allocation
Randomized
Ages
15 Years and older
Sex
All
01

Study summary

  • To compare the quality of Life using AQLQ (s) questionnaire after 4 weeks of Montelukast.
Read the detailed description

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.

02

Conditions studied

  • Asthma

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Keywords

  • Quality of Life
  • Asthma control test
  • Montelukast
  • Asthma
03

In context

Asthma

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 →

Lead sponsor

PharmEvo Pvt Ltd is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Clinical diagnosis of Asthma
  • Signed Informed Consent

Exclusion criteria

Exclusion Criteria:

  • Previous adverse reaction to montelukast or other leukotriene inhibitor;
  • History of hyper-eosinophilic disorder other than atopic disease;
  • Treatment with montelukast within 4 weeks from randomization;
  • Asthma exacerbation or treatment with prednisone/other systemic steroid within 4 weeks from randomization.
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
180 participants (actual)

Study arms

  • Experimental
    Intervention (Montelukast)

    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

  • Placebo comparator
    Placebo

    Patients in placebo group will receive identical looking drug (placebo) produced by same manufactured.

    Drug: Placebo

Interventions

  • DrugMontelukast

    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

  • DrugPlacebo

    Patients in placebo group will receive identical looking drug (placebo) produced by same manufactured

    Also known as: TEAM

06

What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

  2. Proportion of participants experiencing an adverse event (AE)

    \[Designated as safety issue: Yes\]

    Time frame: 0 days to 4 weeks

07

Study locations

1 site
  • Dr. Nadeem Rizvi
    Karachi, Sindh 75510, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03096327
Lead sponsor
PharmEvo Pvt Ltd
Responsible party
Sponsor
First posted
Mar 30, 2017
Start date
May 1, 2017
Primary completion
Dec 30, 2017
Completion
May 30, 2018
Last update
Jul 9, 2018

Study contacts

Masood Jawaid, MRCS,FCPS
study director · PharmEvo Pvt Ltd

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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