MCT and Capsaicin Provocation Challenge in Diagnosis of Chronic Cough

Allergic Rhinitis Clinical Trial

Official title:

The Usefulness of the Methacholine Challenge Test and Capsaicin Inhalation Cough Challenge in a Prediction of Response to Management in Adults With a Chronic Cough.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03363698
• Other study ID #: BHR in chronic cough
• Status: Completed
• Start date: December 31, 2020
• Est. completion date: December 31, 2020

Study information

• Verified date: June 2021
• Source: Medical University of Warsaw
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of the study is to assess the prevalence of bronchial hyperresponsiveness (BHR) in non-smoking adults with chronic cough and the prevalence of BHR in patients with upper airway cough syndrome (UACS) and gastroesophageal reflux disease (GERD), to evaluate the relationship between BHR and cough reflex sensitivity, to assess the diagnostic accuracy of methacholine challenge test (MCT) in cough variant asthma (CVA) with special regard to its discriminating cut off value between CVA and other causes of chronic cough, particularly GERD, to estimate prognostic value of BHR, fractional exhaled nitric oxide (FeNO) and induced sputum eosinophil count in predicting response to asthma treatment. Patients diagnosed with a chronic cough will undergo the standard diagnostic work-up recommended by experts for patients with a chronic cough, including methacholine challenge test (MCT) and an at least 4-week period of causal treatment. Patients with BHR in MCT will be treated with - in first step B2-agonist and inhaled corticosteroid (ICS) for at least 4 weeks, if improvement is not significant in next steps with leukotriene receptor antagonist (LTRA) or systemic corticosteroid. A good treatment response, evaluated by visual analogue scale (VAS), Leicester Cough Questionnaire (LCQ) and cough challenge will confirm the diagnosis of the disease. A statistical analysis will consist of the frequency of BHR in a chronic cough, correlation between the results of MCT and cough reflex sensitivity in capsaicin inhalation test and cut-off point for MCT to discriminate asthma from other causes of a chronic cough.

Description:

The present study has the following objectives: 1. to assess the prevalence of BHR in non-smoking adults with a chronic cough, 2. to assess the prevalence of BHR in patients with UACS and GERD, 3. to evaluate the relationship between BHR and cough reflex sensitivity, 4. to assess the diagnostic accuracy of MCT in CVA with special regard to its discriminating value between CVA and other causes of a chronic cough, particularly GERD, 5. to estimate prognostic value of BHR, fractional exhaled nitric oxide (FeNO) and induced sputum eosinophil count in predicting response to asthma treatment. The investigated group will consist of 80 non-smoking adults (18-75 years old), who are not treated with angiotensin-converting enzyme inhibitors, with no signs of respiratory infection within six weeks prior to enrolment, with a normal chest radiograph and who are referred to the hospital due to a cough lasting at least eight weeks. After obtaining an informed consent, the diagnostic approach of the most common causes of chronic cough will be performed: a medical history, physical examination, chest radiograph, in some cases chest computed tomography, pulmonary function tests (spirometry, fractional exhaled nitric oxide, methacholine challenge test), laboratory tests (total immunoglobulin E concentration, complete blood count), skin prick tests, induced sputum cell count, computed tomography of the paranasal sinuses and ENT consultation, 24-hour impedance with pH monitoring, videolaryngoscopy and cough challenge with capsaicin. The cough severity will be assessed twice (on admission and after six weeks of causal treatment) using the Visual Analogue Scale (VAS), the Polish version of the Leicester Cough Questionnaire (LCQ) and the capsaicin inhalation cough challenge. If MCT result is positive, CVA will be assumed the cause of a chronic cough and treatment with an inhaled steroid combined with a long-acting beta-agonist will be administered for at least 4 weeks. If no satisfactory response to this treatment is observed, an anti-leukotriene agent or in the next step systemic corticosteroid will be applied. Ineffective treatment with the above-mentioned medications will indicate an opportunity for a different underlying cause of BHR. The estimation the area under a ROC (receiver operating characteristic) curve will be used to determine the optimal cut-off point for the differentiation between asthma and alternate causes of a chronic cough. It is expected to assess the frequency of bronchial hyperresponsiveness in subjects with a chronic cough, to confirm a correlation between the results of MCT and the sensitivity of cough reflex measured in capsaicin inhalation cough challenge. The investigation will probably determine a precise cut-off point for MCT which would allow discriminating asthma from other causes of a chronic cough.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 55
• Est. completion date: December 31, 2020
• Est. primary completion date: December 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Adults patients aged between 18 and 75;

2. Chronic cough lasting more than 8 weeks;

3. Non-smoking (min. 6 months);

4. Not treated with angiotensin-converting enzyme (ACE) inhibitors;

5. Not treated with:

1. inhaled corticosteroids or systemic corticosteroids min. 4 weeks before enrolment,

2. proton pump inhibitors min. 2 weeks before enrolment,

3. antihistaminic drugs 1 week before enrolment;

6. With normal chest radiograph or with insignificant changes in cough pathogenesis

7. Without airway infection in previous 6 weeks.

8. Patients enrolled with informed consent.

Exclusion Criteria:

1. Patients under 18 years old and above 75 years old;

2. Smokers (actual or ex-smokers shorter than 6 weeks);

3. Therapy with corticosteroids (inhaled or systemic) for last 4 weeks, proton pump inhibitors for 2 weeks, antihistaminic drug for 1 week before enrolment;

4. Airway infection 6 weeks preceding enrolment or during study - re-attempt to enroll after 6 weeks

Related Conditions & MeSH terms

• Allergic Rhinitis
• Cough
• Cough Variant Asthma
• GERD
• Rhinitis
• Rhinitis, Allergic
• Upper-Airway Cough Syndrome

Intervention

Other:
• Cough variant asthma treatment
Evaluation of the treatment response to inhaled corticosteroids, long-acting beta-agonists, montelukast, prednisone.

Locations

Country	Name	City	State
Poland	Department of Internal Medicine, Lung Diseases and Allergy Medical University of Warsaw	Warsaw	Mazowieckie

Sponsors (1)

Lead Sponsor	Collaborator
Medical University of Warsaw

Country where clinical trial is conducted

Poland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The decrease of a cough after cough variant asthma therapy measured by Leicester Cough Questionnaire (LCQ).	Increase in quality of life measured with LCQ min. 1.3 points.	at least 4 weeks of treatment
Primary	The decrease of a cough after cough variant asthma therapy measured by Visual Analogue Scale (VAS).	Reduction of cough intensity measured by VAS: Reduction min. 20 mm in VAS	at least 4 weeks of treatment
Primary	The decrease of a cough after cough variant asthma therapy measured by the cough challenge.	Increase capsaicin concentration causing causing two/five (C2/C5) cough episode in the cough challenge.	at least 4 weeks of treatment