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Trials / Unknown

UnknownNCT05522699

Cough Suppressive Therapy in Patients With Chronic Cough

Cough Suppressive Therapy in Chronic Cough: Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Uppsala University · Academic / Other
Sex
All
Age
20 Years – 75 Years
Healthy volunteers
Not accepted

Summary

In this randomized, placebo-controlled, interventional study on chronic cough a non-pharmacological cough suppressive therapy is the intervention to be studied, with a control group receiving treatment consisting of general healthy lifestyle advice. The following data will be collected before, after and up to six months after treatment: Standardized questionnaires for diagnosis of background factors, Leicester Cough Questionnaire (LCQ), Work Ability Index (WAI), and cough frequency as well as lung function and biomarkers. The primary treatment effect measurement will be changes in chronic cough-related quality of life, measured by the Leicester Cough Questionnaire (LCQ).

Detailed description

The study will be carried out in collaboration between respiratory physicians, clinical physiologists, physiotherapists, speech- and language therapists and gastroenterologists. The primary hypothesis of the planned study is: The cough suppressive therapy improves chronic cough-related quality of life and work ability, and is sustained over six months after treatment. The secondary hypotheses of the planned study are: Treatment of chronic cough by the cough suppressive therapy can reduce cough frequency (measured by an automated cough detector), airway inflammation and airway resistance. Baseline differences in clinical findings, biomarkers and physiologic measurements predict different treatment effects. The following data will be collected before and after treatment: * Standardized questionnaires for diagnosis of background factors and cough duration, LCQ, WAI, questions on sick leave days, voice disturbance questionnaire. * Physiological measurements: Spirometry with reversibility test, impulse oscillometry before and after provocation with hypertonic saline inhalation. 24 hours cough frequency analysis, voice analysis. * Biomarkers: Fractional exhaled nitric oxide (FeNO), blood-eosinophils and eosinophil cationic protein in serum, proteomics in particles in exhaled air (PExA)

Conditions

Interventions

TypeNameDescription
BEHAVIORALCough suppressive therapyThe cough suppressive therapy based on the treatment regime "Physiotherapy, and speech and language therapy intervention for patients with refractory chronic cough (PSALTI) developed by S. Chamberlain et al (Thorax. 2017 Feb;72(2):129-136).
BEHAVIORALGeneral healthy lifestyle instructionsThe general healthy lifestyle instructions are based on the recommendations from the The Public Health Agency of Sweden.

Timeline

Start date
2022-11-03
Primary completion
2024-08-31
Completion
2024-12-31
First posted
2022-08-31
Last updated
2022-11-08

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05522699. Inclusion in this directory is not an endorsement.