Sensory-Mechanical Responses to Eucapneic Voluntary Hyperventilation and Mannitol
Launched by DR. DIANE LOUGHEED · Apr 4, 2017
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how certain breathing techniques and a medication called Mannitol affect people with specific types of asthma-related coughs, particularly those with cough variant asthma (CVA) and those who cough due to a test called methacholine challenge. The researchers want to see how these treatments cause symptoms like shortness of breath, coughing, and changes in lung function in people with these conditions compared to healthy individuals without asthma or chronic cough.
To participate in this trial, you must be between 18 and 65 years old and have either CVA or a cough triggered by methacholine but with normal airway sensitivity. Healthy individuals within the same age range who have no history of asthma or chronic cough are also eligible. Participants can expect to undergo specific breathing challenges and tests to measure their lung responses. It's important to note that if you've had a recent asthma flare-up or have certain medical issues, you may not be able to join. Overall, this study aims to improve our understanding of how these treatments work for people with chronic coughs related to asthma.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- * Individuals aged 18-65 years of age with CVA and individuals with methacholine-induced cough but normal airway sensitivity. The following definitions will be used:
- • 1. CVA: chronic cough (≥8 weeks) is the sole or predominant symptom and positive methacholine challenge (PC20 ≤ 16 mg/mL) and history of cough responding to specific asthma treatment (such as inhaled steroid or 1 week trial of bronchodilator);
- • 2. Methacholine-induced cough but normal airway sensitivity: chronic cough (≥8 weeks) is the sole or predominant symptom and negative methacholine challenges (PC20 \> 16 mg/mL).
- • Individuals aged 18-65 years of age with no history of asthma or chronic cough.
- Exclusion Criteria:
- • an exacerbation necessitating a change in medication, emergency department visit or hospitalizations within the previous 4 weeks
- • inability to perform acceptable spirometry
- • medical contraindications to methacholine challenge testing
- • smoking history in excess of 10 pack years Note: Previous treatment with inhaled or systemic corticosteroids is not an exclusion criterion; medication use will be recorded and examined in the analysis.
About Dr. Diane Lougheed
Dr. Diane Lougheed is a distinguished clinical trial sponsor known for her expertise in respiratory medicine and her commitment to advancing therapeutic interventions for chronic respiratory diseases. With a robust background in clinical research and a focus on patient-centered outcomes, Dr. Lougheed leads innovative studies that aim to enhance understanding of disease mechanisms and improve treatment efficacy. Her collaborative approach fosters partnerships across multidisciplinary teams, ensuring rigorous study design and ethical conduct. Dr. Lougheed’s contributions to the field are underscored by her dedication to translating research findings into meaningful clinical practice, ultimately striving to improve patient quality of life.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kingston, Ontario, Canada
Patients applied
Trial Officials
M. Diane Lougheed, MD, MSc
Principal Investigator
Department of Medicine, Queen's University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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