Effects of Macrolides on Asthma Control

Sponsor
Euan J Cameron (Other)
Overall Status
Completed
CT.gov ID
NCT00852579
Collaborator
University of Glasgow (Other), NHS Greater Glasgow and Clyde (Other)
77
2
2
29
38.5
1.3

Study Details

Study Description

Brief Summary

Asthma is a common disease in Westernised societies, affecting up to 10% of the population. Corticosteroids are the most effective treatment for asthma but the therapeutic response varies considerably between individuals. A major cause of corticosteroid insensitivity in asthma is cigarette smoking. Active cigarette smoking occurs in over 25% of adults with asthma and a further 25% are ex-smokers. In a series of proof of concept clinical studies the investigators demonstrated for the first time that the efficacy of inhaled and oral corticosteroids is markedly impaired in smokers with asthma and to a lesser extent in ex-smokers with asthma. Active cigarette smoking has other detrimental effects on asthma morbidity including more severe symptoms, increased rates of hospitalisation, and accelerated decline in lung function. Smoking cessation advice is often ineffective because many adult smokers with asthma do not believe that they are personally at risk from their smoking, take many years until stopping smoking and frequently restart smoking after quitting. Alternative or additional drugs to corticosteroids are needed for smokers with asthma who are unable to obtain the clinical benefits associated with stopping smoking. In a proof of concept clinical trial the investigators will test the hypothesis that macrolides improve asthma control and reduce sputum neutrophil counts of smokers with chronic asthma.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Macrolides on Asthma Control, Airway Inflammation and Bacterial Colonisation in Smokers With Asthma.
Study Start Date :
Mar 1, 2009
Actual Primary Completion Date :
Aug 1, 2011
Actual Study Completion Date :
Aug 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Active treatment.

Drug: Azithromycin
Daily dose 250mg

Placebo Comparator: 2

Placebo control group.

Drug: Placebo
Placebo

Outcome Measures

Primary Outcome Measures

  1. Peak expiratory flow rate. [12 weeks]

Secondary Outcome Measures

  1. Spirometry [12 weeks]

  2. Asthma control score [12 weeks]

  3. Average of last 7 days PEF measurements [12 weeks]

  4. Sputum cell counts [12 weeks]

  5. Fraction of expired nitric oxide [12 weeks]

  6. Airway responsiveness to methacholine [12 weeks]

  7. Exacerbation rates [12 weeks]

  8. Cough score [12 weeks]

  9. Diary symptom score [12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Diagnosis of asthma

  • Age 18-70

  • Current smoker

  • Duration of symptoms >1yr with stability for 4 weeks

  • Able to maintain asthma without exacerbations during run in period

  • Able to wean off other asthma medication

Exclusion Criteria:
  • Ex-smokers or never smokers

  • Planning to quit smoking during duration of trial

  • Patients with unstable asthma

  • Patients with current epilepsy, psychosis or history of significant atrial or ventricular tachyarrhythmia

  • Corrected QT-interval greater than 450msec in women, 430msec in men

  • Low potassium levels. If can be corrected then screening can continue with confirmation of normal levels prior to taking study medication

  • Liver disease (ALT and/or AST levels 2 or more times ULN)

  • Significant renal disease (Creatinine or urea levels 2 or more times ULN)

  • Any previous severe adverse reactions to macrolides

  • Patients who are known to have specific IgE sensitivity or skin test positivity to grass pollen and a history of worsening of asthma due to hay fever will not be recruited from mid May to the end of July

  • Upper or lower respiratory tract infection in the 4 weeks prior to randomisation. Run in period can be prolonged in this situation to have 4 weeks with no respiratory infection prior to randomisation.

  • Patients who require medications known to interact with azithromycin

  • On other immunosuppressants or chronic antibiotics

  • Weight less than 45kg

  • Frequent asthma exacerbations (greater than 4) requiring oral corticosteroids in the year prior to randomisation

  • Current or past diagnosis of allergic-bronchopulmonary-aspergillosis

  • Pregnancy and breast feeding

  • Mental impairment or language difficulties that makes informed consent not possible

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gartnavel General Hospital Glasgow United Kingdom G12 0YN
2 Crosshouse Hospital Kilmarnock United Kingdom KA2 0BE

Sponsors and Collaborators

  • Euan J Cameron
  • University of Glasgow
  • NHS Greater Glasgow and Clyde

Investigators

  • Principal Investigator: Neil C Thomson, FRCP, University of Glasgow

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Euan J Cameron, Clinical Research Fellow - Respiratory Medicine, University of Glasgow
ClinicalTrials.gov Identifier:
NCT00852579
Other Study ID Numbers:
  • AR010
  • EUDRACT 2008-007240-34
  • MRC Grant G0701626
  • NRES 09/S0703/23
First Posted:
Feb 27, 2009
Last Update Posted:
Oct 19, 2011
Last Verified:
Oct 1, 2011
Keywords provided by Euan J Cameron, Clinical Research Fellow - Respiratory Medicine, University of Glasgow
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 19, 2011