An Open Label Trial of Azithromycin in Chronic Productive Cough (AZCC)
Primary Purpose
Chronic Cough
Status
Unknown status
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Azithromycin
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Cough focused on measuring Productive, Cough, Bronchitis, Azithromycin
Eligibility Criteria
Inclusion Criteria:
- Age 18 and over
- Male or female
- Non-smokers for 10 years and <20 pack year equivalents in total
- Persistent productive cough for > 3 months in duration
- Use of effective contraception Acceptable contraceptive methods include: established use of oral, injected or implanted hormonal methods; placement of an intrauterine device (IUD) or intrauterine system (IUS); condom or occlusive cap (diaphragm or cervical/vault caps) with spermicide; true abstinence (when this is in line with the preferred and usual lifestyle of the participant); or vasectomised partner.
Exclusion Criteria:
- History of obvious inhaled irritant exposure
- Evidence of primary or secondary immunodeficiency.
- Clinically important bronchiectasis on HRCT scan
- Prolonged QT interval on ECG or significant cardiac pathology prior to commencing azithromycin
- Abnormal LFT's (greater than 2x upper limit of normal)
- Hypersensitivity to azithromycin or any macrolide/ketolide antibiotic
- Pregnancy or intent to become pregnant during course of study
- Contra-indication to bronchoscopy (as per British Thoracic Society Guidelines)
Sites / Locations
- Respiratory Research UnitRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Azithromycin
Arm Description
250mg azithromycin three times weekly for 12 weeks
Outcomes
Primary Outcome Measures
Change from baseline in cough on the Leicester Cough Questionnaire (LCQ) score at week 12
Secondary Outcome Measures
Change from baseline in sputum colour (as per previously validated commercially available graded sputum colour chart) at week 12
Change from baseline in exhaled nitric oxide level (ppm) at week 24
Change from baseline in FEV1 (ml) at week 24
Change from baseline in sputum volume (ml) at week 12
Full Information
NCT ID
NCT02196493
First Posted
July 10, 2014
Last Updated
February 17, 2016
Sponsor
University of Nottingham
1. Study Identification
Unique Protocol Identification Number
NCT02196493
Brief Title
An Open Label Trial of Azithromycin in Chronic Productive Cough
Acronym
AZCC
Official Title
An Open Label Trial of Azithromycin in Chronic Productive Cough
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Unknown status
Study Start Date
December 2013 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nottingham
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
We have noticed a group of patients presenting with a longstanding wet cough which has often been treated as asthma. The cough is productive of sputum which frequently contains bacteria, but does not resolve with standard antibiotic treatment.
A very similar cough is seen in subjects who smoke, have exposure to airbourne dusts or chemicals or have a condition known as bronchiectasis, but these problems have already been excluded.
We have found that prolonged treatment with an antibiotic called azithromycin is very effective but using azithromycin in this way is not licensed and there is currently no trial evidence to support its use.
This research will evaluate the clinical benefit of low dose azithromycin to determine if this is an effective and safe treatment for these patients. It will also involve a detailed investigation of these patients to determine whether they have enough in common to believe we are describing a new condition.
Detailed Description
We and others have observed a cohort of patients, mainly referred with either poorly controlled asthma despite high dose treatment or suspected bronchiectasis, who give a history of chronic (often 3 months or more) productive cough which improves with antibiotic treatment but quickly relapses. Most deny wheeze and on examination there are often transmitted sounds from mucus in the large airways but no expiratory wheeze typical of asthma. Investigations including spirometry, bronchial challenges, chest X-ray, screen for immunodeficiency and high resolution CT (HRCT) scan exclude recognised causes of productive cough but sputum culture is often positive for Haemophilus influenzae although sometimes demonstrates normal respiratory flora despite being markedly purulent.
Due to their efficacy in cystic fibrosis and bronchiectasis we have empirically tried treatment with low dose macrolide antibiotics over 3-6 months often with dramatic benefit. This is however an unproven and unlicensed indication which needs to be more thoroughly evaluated.
The key objective of the study is to determine if 12 weeks treatment of patients with chronic productive cough with low dose azithromycin is both effective and safe.
The secondary objectives of the study are to describe the clinical and pathological features of a cohort of patients who present with chronic productive cough (with no evidence of bronchiectasis, smoking-related chronic bronchitis or immunodeficiency) to determine if these are sufficiently similar to justify a new diagnostic label.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Cough
Keywords
Productive, Cough, Bronchitis, Azithromycin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Azithromycin
Arm Type
Experimental
Arm Description
250mg azithromycin three times weekly for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Other Intervention Name(s)
Zithromax
Intervention Description
250mg azithromycin three times per week for 12 weeks
Primary Outcome Measure Information:
Title
Change from baseline in cough on the Leicester Cough Questionnaire (LCQ) score at week 12
Time Frame
12 weeks after treatment started
Secondary Outcome Measure Information:
Title
Change from baseline in sputum colour (as per previously validated commercially available graded sputum colour chart) at week 12
Time Frame
12 weeks after treatment started
Title
Change from baseline in exhaled nitric oxide level (ppm) at week 24
Time Frame
12 weeks after treatment started
Title
Change from baseline in FEV1 (ml) at week 24
Time Frame
12 weeks after treatment started
Title
Change from baseline in sputum volume (ml) at week 12
Time Frame
12 weeks after treatment started
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 and over
Male or female
Non-smokers for 10 years and <20 pack year equivalents in total
Persistent productive cough for > 3 months in duration
Use of effective contraception Acceptable contraceptive methods include: established use of oral, injected or implanted hormonal methods; placement of an intrauterine device (IUD) or intrauterine system (IUS); condom or occlusive cap (diaphragm or cervical/vault caps) with spermicide; true abstinence (when this is in line with the preferred and usual lifestyle of the participant); or vasectomised partner.
Exclusion Criteria:
History of obvious inhaled irritant exposure
Evidence of primary or secondary immunodeficiency.
Clinically important bronchiectasis on HRCT scan
Prolonged QT interval on ECG or significant cardiac pathology prior to commencing azithromycin
Abnormal LFT's (greater than 2x upper limit of normal)
Hypersensitivity to azithromycin or any macrolide/ketolide antibiotic
Pregnancy or intent to become pregnant during course of study
Contra-indication to bronchoscopy (as per British Thoracic Society Guidelines)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthew Martin, MBChB
Phone
01158231935
Email
matthew.martin@nottingham.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tim Harrison, MD, FRCP
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
Respiratory Research Unit
City
Nottingham
State/Province
Nottinghamshire
ZIP/Postal Code
NG5 1PB
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthew Martin, MBChB
Phone
01158231935
First Name & Middle Initial & Last Name & Degree
Tim Harrison, MD, FRCP
First Name & Middle Initial & Last Name & Degree
Matthew Martin, MBChB MRCP
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30722097
Citation
Martin MJ, Lee H, Clayton C, Pointon K, Soomro I, Shaw DE, Harrison TW. Idiopathic chronic productive cough and response to open-label macrolide therapy: An observational study. Respirology. 2019 Jun;24(6):558-565. doi: 10.1111/resp.13483. Epub 2019 Feb 5.
Results Reference
derived
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An Open Label Trial of Azithromycin in Chronic Productive Cough
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