Trials / Completed
CompletedNCT03380975
Role of Montelukast in Asthma and Allergic Rhinitis Patients
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 600 (actual)
- Sponsor
- Clinision · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
To determine the effect of Montelukast in Asthma and Allergic rhinits patients
Detailed description
Montelukast is a potent and selective blocker of the CysLT1 receptor. Accordingly, a recent study has shown that Montelukast can improve symptoms of seasonal allergic rhinitis and asthma in patients with both diseases. For treatment of 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. Asthma and allergic rhinitis have been linked clinically for many years as "one airway one diseases". Patients with allergic asthma and rhinitis are significantly more likely to experience asthma attacks compared to patients with asthma alone. Side effects most commonly reported above placebo included headache, otitis media, upper respiratory infection, and pharyngitis
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Montelukast 10mg | Montelukast is an orally active compound which binds with high affinity and selectivity to the CysLT1 receptor. Montelukast inhibits physiologic actions of LTD4 at the CysLT1 receptor without any agonist activity. As a result, bronchoconstriction is inhibited with decreased airway and blood eosinophil's leading to improved control over asthma and allergic rhinitis. Montelukast should be taken once daily in the evening |
Timeline
- Start date
- 2018-08-28
- Primary completion
- 2019-03-25
- Completion
- 2019-06-30
- First posted
- 2017-12-21
- Last updated
- 2020-01-03
Locations
1 site across 1 country: Pakistan
Source: ClinicalTrials.gov record NCT03380975. Inclusion in this directory is not an endorsement.