Montelukast for Postinfectious Cough
Primary Purpose
Cough
Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Montelukast
Sponsored by
About this trial
This is an interventional treatment trial for Cough
Eligibility Criteria
Inclusion Criteria:
- Cough is the main or only clinical symptom and was persistent for 3-8 weeks
Chest X-ray reveals no noticeable pathological changes
- 18 year old, regardless of gender and ethical background
- Not taking angiotensin-converting enzyme inhibitor
- Patients must join the programme voluntarily and are able to attend examination and follow-up sessions
Exclusion Criteria:
- Patients diagnosed with allergic rhinitis, chronic nasosinusitis or bacterial respiratory tract infections
- Patients diagnosed with severe reportorial disease of other severe systemic disease
- Patients who are allergic to any drugs to be tested
- Patients who are non-cooperative during examination sessions or other steps of the trial
- Patients who are not able to or refuse to sign consent
Sites / Locations
- Kewu HuangRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Experimental: Montelukast
Placebo Comparator
Arm Description
Patients in experimental treatment arm were given Montelukast Sodium Tablets (p.o., 10mg, q.d.) .All treatment regimens lasted for 10 days and no other antitussive/decongestant or bronchodilators are given to any patients.
Patients in placebo treatment arm were given placebo tablets(main excipient lactose monohydrate,p.o., 10mg, q.d.). All treatment regimens lasted for 10 days and no other antitussive/decongestant or bronchodilators are given to any patients.
Outcomes
Primary Outcome Measures
Change in Leicester Cough Questionnaire(LCQ) total and domain scores at 10 days post randomisation
Secondary Outcome Measures
cough visual analogue scale scores post randomisation(area under the curve)
Change in Leicester Cough Questionnaire(LCQ) physical,psychological and social domain scores at 10 days post randomisation
Full Information
NCT ID
NCT02352545
First Posted
January 16, 2015
Last Updated
January 28, 2015
Sponsor
Beijing Chao Yang Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02352545
Brief Title
Montelukast for Postinfectious Cough
Official Title
Montelukast for Postinfectious Cough in Adults
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
August 2014 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
October 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Chao Yang Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Cough is a common symptom of respiratory medicine clinic patients, which has complex etiology and wide-ranging. Cough is usually divided into three categories by time: acute cough, subacute cough and chronic cough. Subacute has a 3~8 weeks course of disease. Its main etiology is postinfectious cough, which is mostly secondary to viral infection.Considering its overexpression in postinfectious patient, Cysteinyl leukotriene (CysLTs) plays a role in gathering eosinophils to respiratory. The level of FENO has a significant correlation with inflammatory airway eosinophils. While CysLTs overexpressed in vivo, the level of FENO may increase. Montelukast, as CysLTs-receptor-1 antagonists, plays a role of controlling airway inflammation and decrease airway high activity by suppressing the biological activity of CysLTs. It is effective in theory to therapy sub-acute cough by Montelukast, to short the course and to relieve cough symptoms as soon as possible. The aim is to research whether FENO can be used as a biomarker to optimized treatment regimen of sub-acute cough.
Detailed Description
Patients in electrical treatment arm were given Montelukast Sodium Tablets (p.o., 10mg, q.d.) . Patients in placebo treatment arm were given placebo tablets(main excipient lactose monohydrate,p.o., 10mg, q.d.).All treatment regimens lasted for 10 days and no other antitussive/decongestant or bronchodilators are given to any patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cough
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental: Montelukast
Arm Type
Experimental
Arm Description
Patients in experimental treatment arm were given Montelukast Sodium Tablets (p.o., 10mg, q.d.) .All treatment regimens lasted for 10 days and no other antitussive/decongestant or bronchodilators are given to any patients.
Arm Title
Placebo Comparator
Arm Type
Placebo Comparator
Arm Description
Patients in placebo treatment arm were given placebo tablets(main excipient lactose monohydrate,p.o., 10mg, q.d.). All treatment regimens lasted for 10 days and no other antitussive/decongestant or bronchodilators are given to any patients.
Intervention Type
Drug
Intervention Name(s)
Montelukast
Intervention Description
Patients in experimental treatment arm were given Montelukast Sodium Tablets (p.o., 10mg, q.d.) .
Primary Outcome Measure Information:
Title
Change in Leicester Cough Questionnaire(LCQ) total and domain scores at 10 days post randomisation
Time Frame
10 days
Secondary Outcome Measure Information:
Title
cough visual analogue scale scores post randomisation(area under the curve)
Time Frame
10 days
Title
Change in Leicester Cough Questionnaire(LCQ) physical,psychological and social domain scores at 10 days post randomisation
Time Frame
10 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cough is the main or only clinical symptom and was persistent for 3-8 weeks
Chest X-ray reveals no noticeable pathological changes
18 year old, regardless of gender and ethical background
Not taking angiotensin-converting enzyme inhibitor
Patients must join the programme voluntarily and are able to attend examination and follow-up sessions
Exclusion Criteria:
Patients diagnosed with allergic rhinitis, chronic nasosinusitis or bacterial respiratory tract infections
Patients diagnosed with severe reportorial disease of other severe systemic disease
Patients who are allergic to any drugs to be tested
Patients who are non-cooperative during examination sessions or other steps of the trial
Patients who are not able to or refuse to sign consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kewu Huang, M.D.
Phone
86-10-85231167
Email
kewuhuang@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Min Liu, Master
Phone
86-0-13522226189
Email
stream_1980@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kewu Huang, M.D.
Organizational Affiliation
Beijing Chao Yang Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Kewu Huang
City
China
State/Province
Beijing
ZIP/Postal Code
100190
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kewu Huang, M.D.
Phone
86-10-85231167
Email
kewuhuang@126.com
First Name & Middle Initial & Last Name & Degree
Min Liu, Master
Phone
86-0-13522226189
Email
stream_1980@163.com
12. IPD Sharing Statement
Citations:
PubMed Identifier
15358710
Citation
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Results Reference
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PubMed Identifier
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Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Montelukast for Postinfectious Cough
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