Asthma, Cough
Conditions
Keywords
Mannitol, Bronchoconstriction, Airway nerve function, Cough, Diagnostic Test, Osmolarity, Salbutamol
Brief summary
The study aim is to investigate if changes in osmolarity using mannitol challenge can evoke coughing reproducibly in mild allergic asthmatics compared with healthy controls and if salbutamol can affect this. Phase 1 of this study is a reproducibility analysis of cough dose response to mannitol in a cohort of mild allergic asthmatics and healthy controls. Phase 2 is a double-blind, placebo-controlled analysis in mild allergic asthmatics assessing the effects of salbutamol on mannitol induced cough.
Detailed description
The study will have a maximum of 4 visits separated by at least 24 hours. The first 2 visits will determine eligibility. All eligible subjects will be invited back for a third visit, and only subjects with mild allergic asthma will be invited back for a fourth visit. Screening Period (Visits 1 and 2) - For All Subjects Eligible subjects will be identified during the initial screening procedures with measures of spirometry, hyperresponsiveness to methacholine, complete history, physical examination, allergen skin test, and mannitol cough challenge. The screening procedures will be conducted over 2 separate visits. Reproducibility (Visit 3) - For Healthy Controls Ten normal healthy controls meeting study eligibility will return for visit 3. This visit must be at least 24h after the mannitol test at visit 1. These data will be used for assessing reproducibility of the mannitol induced coughs; Emax and the median effective dose (ED50). Effects of Salbutamol (Visit 3 and 4) - For Mild Allergic Asthma Subjects Ten subjects with mild allergic asthma will return for visit 3 and 4. These visits must be at least 24h apart and no longer than 7 days. Mild allergic asthmatics will first receive salbutamol 2.5mg or saline placebo via a nebuliser and 15 mins later the forced expiratory volume at one second (FEV1) measured. Subjects will then undergo a mannitol cough challenge exactly like the previous mannitol cough challenges. These data will be used for determining the effects of salbutamol on mannitol-induced bronchoconstriction and cough. Visit Windows Each visit must be separated by a minimum of 24 hours, and a maximum of 7 days. Study visits can be performed in the morning or afternoon, however for each subject the timing should be consistent with Visits 2 at the same time of day ± 2 hours
Interventions
OTHERMannitol
Mannitol-Induced Cough Challenge
Nebulized salbutamol given prior to Mannitol-Induced Cough Challenge
Nebulized 0.9% saline given prior to Mannitol-Induced Cough Challenge
Sponsors
Syntara
AllerGen NCE Inc.
McMaster University
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Intervention model description
This is a mechanistic study. The first part of the study (mild allergic asthmatics and healthy controls) is to determine reproducibility of dose responses to mannitol-induced coughs. The second part of the study (mild asthmatics only) is to determine the effect of salbutamol on mannitol-induced coughs. Salbutamol or placebo will be delivered following a mannitol cough challenge in a randomized, double-blind crossover design.
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
1. Able to understand and give written informed consent 2. Male and female volunteers 18 through 65 years of age. 3. Positive skin-prick test to common aeroallergens (mild allergic asthmatic subjects) 4. Asthma as determined by methacholine provocative concentration causing a 20% fall (PC20) ≤16 mg/ml for mild allergic asthmatic subjects; no airway hyperresponsiveness as determined by methacholine PC20\>16mg/ml for normal healthy controls. 5. Baseline FEV1 ≥ 70% of the predicted value for mild allergic asthmatic subjects; baseline FEV1≥ 80% of the predicted value for normal healthy controls. 6. Demonstrate cough response to inhaled mannitol
Exclusion criteria
1. Current or former smoker with \>10-pack-year history 2. Current or previous history of other significant respiratory disease 3. Significant systemic disease, including history of current malignancy or autoimmune disease 4. Asthma exacerbation or upper/lower respiratory tract infection within the previous 8 weeks 5. Pregnancy 6. Use of corticosteroids within 28 days prior to the first study visit. 7. Use of nonsteroidal anti-inflammatory drugs (NSAIDs) within 48 hours of study visits or aspirin with 7 days of study visits 8. Use of antihistamines including those in cold and allergy medications within 72 hours of study visits 9. Chronic use of other medication for treatment of allergic lung disease other than short-acting β2-agonists. 10. Use of caffeine-containing products within 4 hours of study visits 11. Use of Angiotensin converting enzyme inhibitors (ACE inhibitors) 12. Any centrally acting medication which in the view of the investigator could alter the sensitivity of the cough reflex including but not restricted to tricyclic anti-depressants, pregabalin, gabapentin, codeine, tramadol, or any other opioid. 13. Lung disease other than mild to moderate allergic asthma, for mild allergic asthmatic subjects; no lung disease for normal healthy controls. 14. Unwillingness or inability to comply with the study protocol for any other reason.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| ED50 dose response curve | Through study completion, an average of one year | Median effective dose |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| ED50 (post-bronchodilator) dose response curve | Through study completion, an average of one year | Median effective dose |
Countries
Canada
Outcome results
None listed