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RECRUITINGOBSERVATIONAL

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance

The Effect of Anti-IL17 on Airway Hyperresponsiveness and Resistance: a Longitudinal Cohort Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This observational longitudinal cohort study aims to assess the effect of monoclonal antibodies targeting interleukin 17 (anti-IL-17) on airway hyperreactivity and airway resistance. The study involves adult participants suffering from dermatological or rheumatological illness, who are planning to start treatment with monoclonal antibodies targeting interleukin 17 as a part of the treatment of these diseases. The primary outcome of this study will be changes in airway hyperresponsiveness to methacholine challenge reported as response-dose-ratio before and after initiation of anti-IL17 treatment regardless of presence of respiratory disease. Furthermore, the potential effect of anti-IL-17 on airway resistance will be assessed using conventional spirometry for measuring changes in FEV1 and Airwave oscillometry. A reduced degree of airway hyperreactivity and airway resistance after initiating ani-IL-17 could indicate effectiveness of anti-IL-17 in asthma patients which would have to be examined further in a population of asthma patients.

Who May Be Eligible (Plain English)

Who May Qualify: - Patients planning to start treatment with anti-IL-17 antibodies Who Should NOT Join This Trial: - Current pregnancy - FEV1 \< 1.5L or less than 60% of predicted value expected. - Previous anaphylactic shock or severe allergic reaction to medicine - Uncontrolled hypertension - Myocardial infarction or stroke within the last 3 months - Known aortic aneurysm - Recent eye surgery or risk of elevated intracranial pressure - Treatment with systemic corticosteroids within 6 weeks Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Patients planning to start treatment with anti-IL-17 antibodies Exclusion Criteria: * Current pregnancy * FEV1 \< 1.5L or less than 60% of predicted value expected. * Previous anaphylactic shock or severe allergic reaction to medicine * Uncontrolled hypertension * Myocardial infarction or stroke within the last 3 months * Known aortic aneurysm * Recent eye surgery or risk of elevated intracranial pressure * Treatment with systemic corticosteroids within 6 weeks

Locations (1)

Respiratory Research Unit Hvidovre Department of Respiratory Medicine, Copenhagen University Hospital
Hvidovre, Capital Region, Denmark