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Montelukast for Persistent Cough in Young People and Adults (MAC)

Primary Purpose

Persistent Cough, Whooping Cough

Status
Unknown status
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Montelukast
Placebo
Sponsored by
University of Oxford
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Cough focused on measuring Montelukast, Persistent cough, Adults, Double-blind randomised placebo controlled trial

Eligibility Criteria

16 Years - 49 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or Female, aged 16 years to 49 years inclusive.
  • Presenting with a persistent cough of 2-8 weeks' duration without an established diagnosis (e.g. asthma, gastro-oesophageal reflux).
  • Able to complete cough diary and study questionnaires.

Exclusion Criteria:

  • There is a contraindication to montelukast.
  • Chronic severe disease which may cause persistent cough (eg cystic fibrosis, bronchiectasis, cardiac failure).
  • Immunodeficiency/immunocompromised state.
  • Pregnancy.
  • Breastfeeding.
  • Current smoker (i.e. stopped smoking less than 6 months ago).
  • Regular medication associated with persistent cough (ACE inhibitors).
  • The individual is in another clinical research study.

Sites / Locations

  • University of Oxford

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Montelukast

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Change in Leicester Cough Questionnaire (LCQ) total score at 2 and 4 weeks post randomisation.

Secondary Outcome Measures

Change in Leicester Cough Questionnaire (LCQ) physical, psychological and social domain scores at 2 and 4 weeks post randomisation.
Overall cough severity according to cough visual analogue scale (VAS) scores over the 2-week period post randomisation (area under the curve).
Paroxysmal cough severity over the 2-week period post randomisation (area under the curve).
Proportions of participants reporting cessation of cough at 2 and 4 weeks post randomisation.
Recruitment rate among young people and adults presenting with acute persistent cough.
Follow-up rates at 2 weeks and 4 weeks post randomisation.
Medication adherence rates at 2 and 4 weeks post randomisation.
Prevalence of whooping cough among participants.
Correlations between subjective cough outcome measures (diary-recorded paroxysms of cough, cough visual analogue scale score and exercise-related cough score) and objective cough frequency measured using the Leicester Cough Monitor.
Proportions of participants undergoing further intervention (re-consultation, investigation, prescription of other medication).
Patient notes will be reviewed in this time frame
Proportions of participants with adverse events.

Full Information

First Posted
January 17, 2011
Last Updated
October 8, 2012
Sponsor
University of Oxford
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1. Study Identification

Unique Protocol Identification Number
NCT01279668
Brief Title
Montelukast for Persistent Cough in Young People and Adults
Acronym
MAC
Official Title
A Double Blind Randomised Placebo Controlled Trial of Montelukast in the Treatment of Acute Persistent Cough in Young People and Adults in Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Unknown status
Study Start Date
May 2011 (undefined)
Primary Completion Date
October 2012 (Anticipated)
Study Completion Date
November 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Oxford

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Persistent cough is a common symptom, accounting for about 20% of referrals to outpatient chest clinics. Most coughs are caused by self-limiting viral infections such as the common cold. However, 1 in 4 people with a viral infection develop a persistent cough, which can go on for several weeks. Whooping cough is a common cause of persistent cough in young people and adults. Although the whooping cough vaccine gives lifelong protection against severe infection, it does not appear to give such long-term protection against milder infections, which can make someone cough for many weeks. There are currently no proven efficacious treatments for persistent cough following either a viral infection or infection with whooping cough. Montelukast is a medication which is already licensed for the treatment of asthma. It works by blocking the action of chemicals called leukotrienes, which make the airways of people with asthma inflamed and sensitive. There is strong evidence to suggest that leukotrienes are also involved in causing persistent cough following viral or whooping cough infection. Montelukast may therefore also help settle persistent coughs in these settings. Over 18 months, we will recruit patients aged 16-49 years with a cough lasting 2-8 weeks from general practices in England. An oral fluid sample will be taken from each participant to be tested for whooping cough. Participants will be randomly allocated to receive a 28-day course of montelukast or placebo tablets and asked to complete a daily cough diary for two weeks. They will be assessed after two weeks by their GP (face-to-face) and after four weeks by another member of practice clinical staff (telephone). Some participants will be given a 24-hour cough monitor to wear on study entry and at two-week follow-up. This study will be funded by the National Institute for Health Research's School of Primary Care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Cough, Whooping Cough
Keywords
Montelukast, Persistent cough, Adults, Double-blind randomised placebo controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
276 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Montelukast
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Montelukast
Other Intervention Name(s)
Singulair
Intervention Description
10mg tablets, once per day for 28 days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
tablets, once per day for 28 days.
Primary Outcome Measure Information:
Title
Change in Leicester Cough Questionnaire (LCQ) total score at 2 and 4 weeks post randomisation.
Time Frame
2 and 4 weeks post randomisation
Secondary Outcome Measure Information:
Title
Change in Leicester Cough Questionnaire (LCQ) physical, psychological and social domain scores at 2 and 4 weeks post randomisation.
Time Frame
2 and 4 weeks post randomisation
Title
Overall cough severity according to cough visual analogue scale (VAS) scores over the 2-week period post randomisation (area under the curve).
Time Frame
2 weeks post randomisation
Title
Paroxysmal cough severity over the 2-week period post randomisation (area under the curve).
Time Frame
2 weeks post randomisation
Title
Proportions of participants reporting cessation of cough at 2 and 4 weeks post randomisation.
Time Frame
2 and 4 weeks post randomisation
Title
Recruitment rate among young people and adults presenting with acute persistent cough.
Time Frame
End of study
Title
Follow-up rates at 2 weeks and 4 weeks post randomisation.
Time Frame
2 weeks and 4 weeks post randomisation.
Title
Medication adherence rates at 2 and 4 weeks post randomisation.
Time Frame
2 and 4 weeks post randomisation
Title
Prevalence of whooping cough among participants.
Time Frame
End of study
Title
Correlations between subjective cough outcome measures (diary-recorded paroxysms of cough, cough visual analogue scale score and exercise-related cough score) and objective cough frequency measured using the Leicester Cough Monitor.
Time Frame
2 and 4 weeks post randomisation
Title
Proportions of participants undergoing further intervention (re-consultation, investigation, prescription of other medication).
Description
Patient notes will be reviewed in this time frame
Time Frame
4 - 8 weeks
Title
Proportions of participants with adverse events.
Time Frame
End of study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or Female, aged 16 years to 49 years inclusive. Presenting with a persistent cough of 2-8 weeks' duration without an established diagnosis (e.g. asthma, gastro-oesophageal reflux). Able to complete cough diary and study questionnaires. Exclusion Criteria: There is a contraindication to montelukast. Chronic severe disease which may cause persistent cough (eg cystic fibrosis, bronchiectasis, cardiac failure). Immunodeficiency/immunocompromised state. Pregnancy. Breastfeeding. Current smoker (i.e. stopped smoking less than 6 months ago). Regular medication associated with persistent cough (ACE inhibitors). The individual is in another clinical research study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anthony R Harnden
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Oxford
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX3 7LF
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
16829538
Citation
Harnden A, Grant C, Harrison T, Perera R, Brueggemann AB, Mayon-White R, Mant D. Whooping cough in school age children with persistent cough: prospective cohort study in primary care. BMJ. 2006 Jul 22;333(7560):174-7. doi: 10.1136/bmj.38870.655405.AE. Epub 2006 Jul 7.
Results Reference
background
PubMed Identifier
12668799
Citation
Birring SS, Prudon B, Carr AJ, Singh SJ, Morgan MD, Pavord ID. Development of a symptom specific health status measure for patients with chronic cough: Leicester Cough Questionnaire (LCQ). Thorax. 2003 Apr;58(4):339-43. doi: 10.1136/thorax.58.4.339.
Results Reference
background
PubMed Identifier
24461900
Citation
Wang K, Birring SS, Taylor K, Fry NK, Hay AD, Moore M, Jin J, Perera R, Farmer A, Little P, Harrison TG, Mant D, Harnden A. Montelukast for postinfectious cough in adults: a double-blind randomised placebo-controlled trial. Lancet Respir Med. 2014 Jan;2(1):35-43. doi: 10.1016/S2213-2600(13)70245-5. Epub 2013 Dec 2.
Results Reference
derived

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Montelukast for Persistent Cough in Young People and Adults

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