Open-label Study of the Effects of Montelukast in Patients With Chronic Cough
Primary Purpose
Coughing
Status
Completed
Phase
Phase 4
Locations
Bulgaria
Study Type
Interventional
Intervention
Montelukast
Sponsored by
About this trial
This is an interventional treatment trial for Coughing
Eligibility Criteria
Inclusion Criteria:
- Patients with chronic cough: cough persisting for more than 8 consecutive weeks
Exclusion Criteria:
- Current use of ACE-inhibitors
- Use of systemic steroids in the last 4 weeks
- COPD
- Pregnancy
- Concomitant severe disease
- Smoking
Sites / Locations
- Clinic of Allergy and Asthma, University Hospital "Alexandrovska"
Arms of the Study
Arm 1
Arm Type
Active Comparator
Arm Label
Montelukast
Arm Description
Montelukast tablets: adults - 10 mg, children - 5mg taken daily for two weeks
Outcomes
Primary Outcome Measures
Difference in the cough reflex parameters (C2 and C5) before and after two weeks of treatment with montelukast
Difference in average scores on modified Leicester Cough Questionnaire (LCQ) before and after two weeks of treatment with montelukast
Secondary Outcome Measures
Difference in pulmonary function parameters (FVC, FEV1, PEF), before and after two weeks of treatment with montelukast
Difference in Exhaled breath temperature (EBT) before and after two weeks of treatment with montelukast
Difference in laboratory markers (CBC, CRP, total IgE, ESP, MPO) before and after two weeks of treatment with montelukast
Full Information
NCT ID
NCT01754220
First Posted
November 3, 2012
Last Updated
December 18, 2012
Sponsor
Association Asthma, Bulgaria
1. Study Identification
Unique Protocol Identification Number
NCT01754220
Brief Title
Open-label Study of the Effects of Montelukast in Patients With Chronic Cough
Official Title
The Effects of Alvokast (Montelukast) in Patients With Chronic Cough
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Association Asthma, Bulgaria
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Montelukast, a leukotriene receptor antagonist, is likely to be effective in the treatment of chronic cough and this could be made objective by measuring cough threshold before and after two weeks of treatment.
Detailed Description
Chronic cough is typically defined as cough that persists for longer than 8 weeks and is the most common presenting symptom in adults who seek medical treatment in an ambulatory setting. Prospective studies have shown that three conditions account for the etiologic cause of chronic cough in the largest part of immunocompetent, nonsmoking patients with normal chest radiograph findings. In order of frequency, they are upper airway cough syndrome (UACS), previously referred to as postnasal drip syndrome (PNDS), asthma and gastroesophageal reflux disease (GERD). UACS comprises many different conditions including PNDS, acute sinusitis, allergic rhinitis, non-allergic rhinitis (postinfectious rhinitis, rhinitis medicamentosa, vasomotor rhinitis, rhinitis due to physical or chemical irritants). Cough occurs in all asthmatics, and in a subset of patients with cough-variant asthma (CVA), it is the only presenting symptom. In these cases it is well controlled with inhaled corticosteroids and beta-2 agonists. GERD is another cause that should be contemplated when anti-tussive or anti-inflammatory/anti-allergic treatment do not render results and when there are presenting symptoms suggestive of it. Moreover, factors like smoking and use of ACE-inhibitors should also be taken into account.
Leukotrienes are very important agents in the inflammatory response. It is known that they are contributing significantly to the pathological processes in asthma. Montelukast is a leukotriene receptor antagonist which blocks the bonding of leukotrienes to their receptors thus inhibiting their inflammatory, bronchoconstrictive and mucosecretory effects. Multiple clinical trials have demonstrated the ability of the leukotriene antagonists to improve symptoms, pulmonary function and bronchial hyperresponsiveness in patients with asthma. However, not much is known about their effects in people with chronic cough. Studies have been carried out in an attempt to find out the effects of montelukast in some forms of chronic cough. Nevertheless, the impact of montelukast on objective parameters such as cough reflex threshold, has not been explored. The investigators also reckon that montelukast will affect exhaled breath temperature - a novel surrogate marker of airway inflammation recognized lately
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coughing
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Montelukast
Arm Type
Active Comparator
Arm Description
Montelukast tablets: adults - 10 mg, children - 5mg taken daily for two weeks
Intervention Type
Drug
Intervention Name(s)
Montelukast
Other Intervention Name(s)
Alvokast
Intervention Description
Montelukast is a leukotriene receptor antagonist
Primary Outcome Measure Information:
Title
Difference in the cough reflex parameters (C2 and C5) before and after two weeks of treatment with montelukast
Time Frame
7 months
Title
Difference in average scores on modified Leicester Cough Questionnaire (LCQ) before and after two weeks of treatment with montelukast
Time Frame
7 months
Secondary Outcome Measure Information:
Title
Difference in pulmonary function parameters (FVC, FEV1, PEF), before and after two weeks of treatment with montelukast
Time Frame
7 months
Title
Difference in Exhaled breath temperature (EBT) before and after two weeks of treatment with montelukast
Time Frame
7 months
Title
Difference in laboratory markers (CBC, CRP, total IgE, ESP, MPO) before and after two weeks of treatment with montelukast
Time Frame
7 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with chronic cough: cough persisting for more than 8 consecutive weeks
Exclusion Criteria:
Current use of ACE-inhibitors
Use of systemic steroids in the last 4 weeks
COPD
Pregnancy
Concomitant severe disease
Smoking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Todor A Popov, MD, Phd
Organizational Affiliation
Association Asthma, Bulgaria
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinic of Allergy and Asthma, University Hospital "Alexandrovska"
City
Sofia
ZIP/Postal Code
1431
Country
Bulgaria
12. IPD Sharing Statement
Citations:
PubMed Identifier
10453852
Citation
Palombini BC, Villanova CA, Araujo E, Gastal OL, Alt DC, Stolz DP, Palombini CO. A pathogenic triad in chronic cough: asthma, postnasal drip syndrome, and gastroesophageal reflux disease. Chest. 1999 Aug;116(2):279-84. doi: 10.1378/chest.116.2.279.
Results Reference
background
PubMed Identifier
12661998
Citation
Paredi P, Caramori G, Cramer D, Ward S, Ciaccia A, Papi A, Kharitonov SA, Barnes PJ. Slower rise of exhaled breath temperature in chronic obstructive pulmonary disease. Eur Respir J. 2003 Mar;21(3):439-43. doi: 10.1183/09031936.03.00061902.
Results Reference
background
PubMed Identifier
24649919
Citation
Mincheva RK, Kralimarkova TZ, Rasheva M, Dimitrov Z, Nedeva D, Staevska M, Papochieva V, Perenovska P, Bacheva K, Dimitrov VD, Popov TA. A real - life observational pilot study to evaluate the effects of two-week treatment with montelukast in patients with chronic cough. Cough. 2014 Mar 20;10(1):2. doi: 10.1186/1745-9974-10-2.
Results Reference
derived
Learn more about this trial
Open-label Study of the Effects of Montelukast in Patients With Chronic Cough
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