A Cross-sectional Study to Measure Cough in Severe Asthma

Asthma Clinical Trial

— CISA  

Official title:

A Cross-sectional Study to Measure Cough in Severe Asthma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03999203
• Other study ID #: B17/03
• Status: Completed
• Phase: N/A
• Start date: October 4, 2017
• Est. completion date: December 30, 2019

Study information

• Verified date: February 2023
• Source: Queen's University, Belfast
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to characterise cough in severe asthma through an observational cross-sectional analysis of patients stratified by inflammatory biomarker profile using a number of subjective and objective cough measurement tools.

Description:

This study will use a combination of subjective and objective cough measures to assess the frequency of cough as well as its related morbidity in severe asthmatics. Comparisons will be made between T2-High, T2-Low and T2-intermediate patients defined using a composite biomarker profile (blood eosinophil count and FeNO) to assess the role of cough in each and these results will be compared to the transcriptomic and proteomic measurements in the RASP-UK where the same biomarker profiling is being used to define clinical sub-groups of severe asthma. This study aims to also improve characterisation of the T2-Low population and identify possible mechanisms for the pathophysiology of this group.

60 patients are expected to be recruited to the study. Patients will be provided with an information sheet and have a telephone follow-up after at least 24 hours to ask if they remain interested in participation and if so, they will then be asked back for a baseline visit.

Three groups of severe asthmatics will be recruited (as described in appropriate section) and undergo the following procedures:

• Demographic details, height, weight, spirometry, FeNO and vital signs

• Patient reported outcomes:

• Asthma Mini-Asthma Quality of Life Questionnaire (mini-AQLQ) - abbreviated version of Juniper AQLQ

• Asthma Control Questionnaire (ACQ-5 (5 questions);

• Leicester Cough Questionnaire, the Cough-specific quality-of-life Questionnaire and Cough Hypersensitivity Questionnaire will be used to assess the impact of cough;

• Visual analogue scales (VAS) for cough (VASc) and urge to cough (VASu) will be used as a measure of cough severity.

• Blood samples - a sample of blood will be taken for whole blood transcriptomic and serum analyses

• Citric acid cough challenge test will be used to measure cough reflex sensitivity in each phenotype.

• Spontaneous sputum sample - if patients produce a sputum sample during spirometry or citric acid challenge, this will be recorded and the sample will be retained for sputum differential cell count and storage of processed soluble components.

• On completing the above procedures, patients will be asked to wear a validated ambulatory cough monitor (Leicester Cough Monitor) for a 24-hour period to assess the frequency of cough and if they agree, will be fully instructed in its use.

Patients will be asked to attend a follow-up visit 2 weeks after baseline. The study procedures will remain the same as visit 1 with the exception of collection of clinical samples.

A mild/moderate population will be recruited and undergo the same procedures as the severe group in a baseline visit. No mild/moderate asthmatics will be asked to attend for a follow-up visit.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 61
• Est. completion date: December 30, 2019
• Est. primary completion date: December 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria (Severe Asthmatics):

1. Ability and willingness to comply with the study procedures

2. Age =18 to =75 years at the time of informed consent

3. Severe asthma (as defined by GINA step 4/5 classification of asthma severity) after a detailed systematic assessment

4. History of asthma treatment with high doses of Inhaled Corticosteroids (=1000 µg beclomethasone dipropionate daily, or equivalent) and an additional controller

5. Three patient groups with severe asthma will be investigated in the study and will be defined as follows:

T2-High Severe Asthmatics (Group A)

• Persistent blood eosinophil count =0.3x10^9/mL and

• Persistent high FeNO levels =30 ppb and

• Adherence to inhaled and oral corticosteroid therapy

T2-Low Severe Asthmatics (Group B)

• Persistent blood eosinophil count =0.2x10^9/Ml and

• Persistent low FeNO levels (<30ppb)

T2 - Intermediate Severe Asthmatics (Group D)

• Persistent blood eosinophil count = 0.3x10^9/mL OR

• Persistent FeNO levels = 30 ppb

As stated above, these measurements are made at each clinic visit as part of routine care and will be available on all subjects prior to Inclusion

6. A chest x-ray or CT scan obtained within 12 months before the time of informed consent and showing no new pathology requiring investigation as a potential cause for their cough

Mild/moderate severe asthmatics (who have received a diagnosis of asthma from a physician and are defined as step 2/3 using the BTS/SIGN classification of severity and ACQ<1.5) aged 18-75 years inclusive will be recruited from general respiratory clinics in the Belfast HSC Trust. Patients must have the ability and willingness to comply with study procedures.

Exclusion Criteria:

1. Baseline FEV1 =50% of predicted or = 1.0L

2. Asthma exacerbation within 28 days before the time of informed consent or during screening

3. Major episode of infection requiring any of the following:

• Admission to hospital for =24 hours within the 28 days before the time of informed consent

• Treatment with intravenous antibiotics within the 28 days before the time of informed consent or during Screening

• Treatment with oral antibiotics within the 14 days before the time of informed consent or during Screening

4. For adults: Active tuberculosis (TB) requiring treatment within the 12 months before the time of informed consent (patients are also required to have no recurrence of symptoms in the 12 months following completion of TB treatment), or

5. Known history of severe clinically significant immunodeficiency, including, but not limited to, human immunodeficiency virus infection and/or currently receiving or have historically received intravenous Ig for treatment for immunodeficiency Note: Immunodeficiency encompasses a wide spectrum of human conditions and/or diseases. A relative IgG deficiency that is thought, but not proven, to be a feature of severe asthma would not be exclusionary for the study.

6. Diagnosis or history of malignancy, or current investigation for possible malignancy

7. Other clinically significant medical disease that is uncontrolled despite treatment or that is likely, in the opinion of the investigator, to require a change in therapy or affect the ability to participate in the study

8. History of alcohol, drug, or chemical abuse that would impair or risk the patient's full participation in the study, in the opinion of the investigator

9. Current smoker or former smoker with a smoking history of >15 pack-years A current smoker is defined as someone who has smoked one or more cigarettes per day (or marijuana or pipe or cigar) for =30 days within the 24 months before the time of informed consent and for whom cotinine testing is positive.

A former smoker is defined as someone who has smoked one or more cigarettes per day (or marijuana or pipe or cigar) for =30 days in his or her lifetime (as long as the 30-day total did not include the 24 months before the time of informed consent) and for whom cotinine testing is negative.

A pack-year is defined as the average number of packs per day times the number of years of smoking.

10. Initiation of or change in allergen immunotherapy within three months before the time of informed consent

11. Treatment with an investigational agent within 30 days of informed consent or 5 half-lives of the investigational agent, whichever is longer

12. Female patients who are pregnant or lactating

Related Conditions & MeSH terms

• Asthma
• Cough

Intervention

Drug:
• Citric acid
Citric Acid cough challenge to be administered to assess the cough reflex sensitivity in patients

Device:
• Leicester Cough monitor
Ambulatory cough monitor to assess cough frequency over a 24 hour period

Other:
• fractional exhaled nitric oxide testing (FeNO)
Measurement of exhaled nitric oxide to give an indication of airway inflammation
• Patient reported outcome measures
A number a patient reported outcome measures will be administered including: Asthma control questionnaire (ACQ-5), mini Asthma Quality of Life Questionnaire (mini AQLQ), Leicester Cough Questionnaire (LCQ), Cough Quality of Life Questionnaire (CQLQ), Cough Hypersensitivity Questionnaire (CHQ) and visual analogue scales for severity og cough (VASc) and Urge to Cough (VASu)

Locations

Country	Name	City	State
United Kingdom	Queen's University Belfast	Belfast

Sponsors (2)

Lead Sponsor	Collaborator
Queen's University, Belfast	King's College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cough Frequency Measurement	Objectively measure cough frequency (measured as hours per hour over a 24 hour monitoring period) in different phenotypes of severe asthma and a mild/moderate control group using a validated ambulatory cough monitor (Leicester Cough Monitor)	Baseline
Primary	Cough Reflex Sensitivity (Citric Acid Cough Challenge)	To objectively measure cough reflex sensitivity in different phenotypes of severe asthma and a mild.moderate control group using citric acid cough challenge testing.; Patients are asked to inhale increasing concentrations of citric acid solutions and the cough response to each is measured in the 15 seconds following. The final outcome endpoint is described as the concentrations needed to cause 2 coughs (C2)	Baseline
Secondary	Asthma Control Questionnaire	Assessment of asthma control using subjective questionnaire (asthma control questionnaire) in different phenotypes of severe asthma. Patient responses graded on likert scale with an average score being calculated. A higher score indicates a worse level of asthma control. Score range 0-6	Baseline
Secondary	Asthma Quality of Life Questionnaire	Assesment of quality of life in asthma as perceived by the patient using this questionnaire in different phenotypes of severe asthma. Patient responses graded on likert scale with an average score being calculated. A higher score indicates a worse level of asthma related quality of life. Score range 1-7	Baseline
Secondary	Leceister Cough Questionnaire	Assessment of quality of life in relation to cough in different phenotypes of severe asthma. Patient responses graded on likert scale with an average score being calculated from different symptoms domains wihtin the questionnaire. A lower score indicates a worse level of cough related quality of life. Score range 3-21	Baseline
Secondary	Cough Quality of Life Questionnaire	Assessment of quality of life in relation to cough in different phenotypes of severe asthma. Patient responses graded on likert scale with a total score being calculated. A higher score indicates a worse level of cough related quality of life. Score range 28-112	Baseline
Secondary	Fractional Exhaled Nitric Oxide (FeNO)		Baseline
Secondary	Blood Eosinophil Count		Baseline